SuccessConsole Output

Started by upstream project "hpo" build number 1699
originally caused by:
 Started by user koehler
Building in workspace /var/lib/jenkins/jobs/hpo.annotations/workspace
Cleaning up /var/lib/jenkins/jobs/hpo.annotations/workspace/.
Deleting /var/lib/jenkins/jobs/hpo.annotations/workspace/misc/hpo
Deleting /var/lib/jenkins/jobs/hpo.annotations/workspace/misc/makefile.prej
Deleting /var/lib/jenkins/jobs/hpo.annotations/workspace/misc/orphanetmapping
Deleting /var/lib/jenkins/jobs/hpo.annotations/workspace/misc/external_orphanet
Updating https://github.com/monarch-initiative/hpo-annotation-data/trunk/rare-diseases@HEAD at revision HEAD
UC        misc/makefile
At revision 3130
[workspace] $ /bin/sh -xe /tmp/hudson5201577627571293778.sh
+ make -C misc
make: Entering directory '/var/lib/jenkins/jobs/hpo.annotations/workspace/misc'
# load orphanet data
mkdir -p external_orphanet
# Employ wget to retrieve all external ontologies as specified
# in external_ontologies. We also ignore lines starting with #
cd external_orphanet ; cat ../external_orphanet.txt | sed "/^#.*$/d" | wget --retry-connrefused -N -i -
--2016-01-13 13:18:45--  http://www.orphadata.org/data/xml/en_product1.xml
Resolving proxy.charite.de (proxy.charite.de)... 141.42.1.215
Connecting to proxy.charite.de (proxy.charite.de)|141.42.1.215|:8080... connected.
Proxy request sent, awaiting response... 200 OK
Length: 20259500 (19M) [text/xml]
Saving to: ‘en_product1.xml’

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 13300K .......... .......... .......... .......... .......... 67% 1.96M 2s
 13350K .......... .......... .......... .......... .......... 67% 4.28M 2s
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 14300K .......... .......... .......... .......... .......... 72% 1010K 2s
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 18200K .......... .......... .......... .......... .......... 92% 1.60M 0s
 18250K .......... .......... .......... .......... .......... 92% 8.55M 0s
 18300K .......... .......... .......... .......... .......... 92% 1.57M 0s
 18350K .......... .......... .......... .......... .......... 93% 3.07M 0s
 18400K .......... .......... .......... .......... .......... 93% 2.91M 0s
 18450K .......... .......... .......... .......... .......... 93% 3.04M 0s
 18500K .......... .......... .......... .......... .......... 93% 2.83M 0s
 18550K .......... .......... .......... .......... .......... 94% 2.91M 0s
 18600K .......... .......... .......... .......... .......... 94% 3.01M 0s
 18650K .......... .......... .......... .......... .......... 94% 1.67M 0s
 18700K .......... .......... .......... .......... .......... 94% 3.07M 0s
 18750K .......... .......... .......... .......... .......... 95% 2.41M 0s
 18800K .......... .......... .......... .......... .......... 95% 3.88M 0s
 18850K .......... .......... .......... .......... .......... 95% 2.38M 0s
 18900K .......... .......... .......... .......... .......... 95% 2.56M 0s
 18950K .......... .......... .......... .......... .......... 96% 3.40M 0s
 19000K .......... .......... .......... .......... .......... 96% 2.27M 0s
 19050K .......... .......... .......... .......... .......... 96% 3.90M 0s
 19100K .......... .......... .......... .......... .......... 96% 1.76M 0s
 19150K .......... .......... .......... .......... .......... 97% 3.58M 0s
 19200K .......... .......... .......... .......... .......... 97% 2.19M 0s
 19250K .......... .......... .......... .......... .......... 97% 3.82M 0s
 19300K .......... .......... .......... .......... .......... 97% 2.35M 0s
 19350K .......... .......... .......... .......... .......... 98% 2.56M 0s
 19400K .......... .......... .......... .......... .......... 98% 3.50M 0s
 19450K .......... .......... .......... .......... .......... 98% 2.25M 0s
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 19750K .......... .......... .......... ....                 100% 2.54M=6.3s

2016-01-13 13:18:52 (3.09 MB/s) - ‘en_product1.xml’ saved [20259500/20259500]

--2016-01-13 13:18:52--  http://www.orphadata.org/data/xml/en_product4.xml
Reusing existing connection to proxy.charite.de:8080.
Proxy request sent, awaiting response... 200 OK
Length: 15118367 (14M) [text/xml]
Saving to: ‘en_product4.xml’

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  7550K .......... .......... .......... .......... .......... 51% 1.47M 4s
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  8150K .......... .......... .......... .......... .......... 55% 1.48M 4s
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  8350K .......... .......... .......... .......... .......... 56% 1.39M 4s
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  9500K .......... .......... .......... .......... .......... 64%  733K 4s
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  9600K .......... .......... .......... .......... .......... 65%  761K 4s
  9650K .......... .......... .......... .......... .......... 65%  756K 4s
  9700K .......... .......... .......... .......... .......... 66% 1.45M 4s
  9750K .......... .......... .......... .......... .......... 66%  744K 4s
  9800K .......... .......... .......... .......... .......... 66%  771K 4s
  9850K .......... .......... .......... .......... .......... 67%  766K 4s
  9900K .......... .......... .......... .......... .......... 67%  739K 4s
  9950K .......... .......... .......... .......... .......... 67% 1.44M 4s
 10000K .......... .......... .......... .......... .......... 68%  770K 3s
 10050K .......... .......... .......... .......... .......... 68%  760K 3s
 10100K .......... .......... .......... .......... .......... 68% 1.47M 3s
 10150K .......... .......... .......... .......... .......... 69%  761K 3s
 10200K .......... .......... .......... .......... .......... 69%  752K 3s
 10250K .......... .......... .......... .......... .......... 69% 1.28M 3s
 10300K .......... .......... .......... .......... .......... 70%  804K 3s
 10350K .......... .......... .......... .......... .......... 70%  778K 3s
 10400K .......... .......... .......... .......... .......... 70% 1.47M 3s
 10450K .......... .......... .......... .......... .......... 71%  761K 3s
 10500K .......... .......... .......... .......... .......... 71% 1.45M 3s
 10550K .......... .......... .......... .......... .......... 71%  685K 3s
 10600K .......... .......... .......... .......... .......... 72% 1.62M 3s
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 10700K .......... .......... .......... .......... .......... 72% 1.43M 3s
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 11500K .......... .......... .......... .......... .......... 78% 1.55M 2s
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 14300K .......... .......... .......... .......... .......... 97%  947K 0s
 14350K .......... .......... .......... .......... .......... 97% 3.46M 0s
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 14450K .......... .......... .......... .......... .......... 98% 1.34M 0s
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 14750K .......... ....                                       100%  468K=11s

2016-01-13 13:19:03 (1.29 MB/s) - ‘en_product4.xml’ saved [15118367/15118367]

FINISHED --2016-01-13 13:19:03--
Total wall clock time: 18s
Downloaded: 2 files, 34M in 17s (1.93 MB/s)
# loads the mapping between orphanet's signs-and-symptoms and HPO
svn checkout https://github.com/obophenotype/human-phenotype-ontology/trunk/src/mappings/ orphanetmapping
A    orphanetmapping/LDDB2HPO-v2.csv
A    orphanetmapping/README_LICENSE.txt
A    orphanetmapping/hp-to-eom-mapping.tsv
A    orphanetmapping/medraMapping.tsv
A    orphanetmapping/onet_hpo.tsv
A    orphanetmapping/term2umls.out
Checked out revision 1028.
# loads the HPO
#wget -N -P hpo http://compbio.charite.de/hudson/job/hpo/lastSuccessfulBuild/artifact/hp/hp.obo
wget -N -P hpo http://build.berkeleybop.org/job/build-hp-edit/lastSuccessfulBuild/artifact/src/ontology/hp.obo
--2016-01-13 13:19:07--  http://build.berkeleybop.org/job/build-hp-edit/lastSuccessfulBuild/artifact/src/ontology/hp.obo
Resolving proxy.charite.de (proxy.charite.de)... 141.42.1.215
Connecting to proxy.charite.de (proxy.charite.de)|141.42.1.215|:8080... connected.
Proxy request sent, awaiting response... 200 OK
Length: 4389201 (4.2M) [application/octet-stream]
Saving to: ‘hpo/hp.obo’

     0K .......... .......... .......... .......... ..........  1% 16.8M 0s
    50K .......... .......... .......... .......... ..........  2% 17.1M 0s
   100K .......... .......... .......... .......... ..........  3% 57.8K 24s
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  3000K .......... .......... .......... .......... .......... 71% 43.0M 1s
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  3550K .......... .......... .......... .......... .......... 83% 95.6M 0s
  3600K .......... .......... .......... .......... .......... 85% 6.28M 0s
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  3800K .......... .......... .......... .......... .......... 89% 47.3M 0s
  3850K .......... .......... .......... .......... .......... 90%  115M 0s
  3900K .......... .......... .......... .......... .......... 92% 52.5M 0s
  3950K .......... .......... .......... .......... .......... 93% 57.0M 0s
  4000K .......... .......... .......... .......... .......... 94% 65.5M 0s
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  4100K .......... .......... .......... .......... .......... 96% 41.7M 0s
  4150K .......... .......... .......... .......... .......... 97% 60.1M 0s
  4200K .......... .......... .......... .......... .......... 99% 90.2M 0s
  4250K .......... .......... .......... ......               100% 73.6M=2.5s

2016-01-13 13:19:14 (1.68 MB/s) - ‘hpo/hp.obo’ saved [4389201/4389201]

mkdir -p hpo
mv hpo/hp.obo hpo/human-phenotype-ontology.obo
java -Xmx1G -jar jarFiles/generateAnnotationFile.jar --orphadata "external_orphanet" --sign-mapping "orphanetmapping/onet_hpo.tsv" --out-folder "." --hpo_ontology "hpo" --berkeley-annotated "../annotated/"
Jan 13, 2016 1:19:14 PM ontologizer.go.OBOParser doParse
INFO: Got 11639 terms and 15300 relations in 106 ms
Details of parsed obo file:
  filename:		hpo/human-phenotype-ontology.obo
  date:			null
  format:		1.2
  term definitions:	11639
Jan 13, 2016 1:19:14 PM ontologizer.go.Ontology assignLevel1TermsAndFixRoot
INFO: Ontology contains a single level-one term (All (HP:0000001)
Jan 13, 2016 1:19:15 PM ontologizer.go.Ontology assignLevel1TermsAndFixRoot
INFO: Ontology contains a single level-one term (Phenotypic abnormality (HP:0000118)
/var/lib/jenkins/jobs/hpo.annotations/workspace/misc/../annotated
.
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...............Reading Orphanet x-ref file...
omim->orphanet mappings: 5689
orphanet->omim mappings: 4243
...done
Reading Orphanet annotation file...
number of Orphanet entries with annotation: 2681
...done
Reading Orphanet-sign to HPO mapping file...
1 > id_signe_55680			Twinning (type unknown)			we do not really need this as a feature do we?
2 > id_signe_55480			Antenatal exposure : anticoagulants		sdoelken	?
3 > id_signe_55180			Antenatal exposure to infectious agent			?
4 > id_signe_23600			Vascular anomalies of skin/mucosae		sdoelken	?
5 > id_signe_24000			Hair and scalp anomalies		sdoelken	??? scalp and hair are not necessaryly closely related in the HP there is no good common ancestor
6 > id_signe_45690			Bone tumefaction/swelling			"do we really need this term? It is very imprecise as to cause and actual appearance of bone ""swelling"" we would rather recommend to use precise terms such as""Neoplasia of the skeletal system"" or ""Thickened cortex of bones""... for those kind of findings"
7 > id_signe_46000			"Anomalies of cartilages, joints and periarticular tissue"			? we have HP:0002763 Abnormality of cartilage and HP:0001367 Abnormality of the joints but we do not group this together the way orphanet does - next common ancestor would be HP:0000924 Abnormality of the musculoskeletal system - which is very general
8 > id_signe_55440			Antenatal exposure : anticonvulsants			?
9 > id_signe_43500			Alexia/agraphia/writing/reading troubles		sdoelken	? HP:0002167 Neurological speech impairment has children HP:0010523 Alexia and HP:0010526 Dysgraphia (and many more)
10 > id_signe_48080			Bone marrow/medullar infiltration		sdoelken	? do we need this
11 > id_signe_55460			Antenatal exposure : iodures		sdoelken	?
12 > id_signe_10420			Hamartoma/tumefaction of the tongue/gingivae/oral mucosa		sdoelken	?
13 > id_signe_35390			Arterial pulse abolition		sdoelken	? does this mean no pulse as in dead?
14 > id_signe_46240			Musculo-tendinous retractions		sdoelken	?
15 > id_signe_20240			Flat palm		sdoelken	what is meant?
16 > id_signe_54350			Asthenia/fatigue/weakness		sdoelken	?
17 > id_signe_55400			Antenatal exposure : antibiotics		sdoelken	?
18 > id_signe_49400			Carbohydrates metabolism anomalies		sdoelken	probinson? what does the metabolic specialist say?
19 > id_signe_54770			Biological inflammatory syndrome/increased erythrocyte sedimentation rate/CRP		sdoelken	we have HP:0003565 Elevated erythrocyte sedimentation rate - I think we need CRP... as well and should expand the HPO structure here - what do you think probinson?
20 > id_signe_46840			Articular click		sdoelken	I don't think we want to have this term...
21 > id_signe_49020			Metabolic decompensation		sdoelken	? probinson ?
22 > id_signe_26020			Respiratory-digestive intersection/aero-digestive cross-roads anomaly			? what exactly does this mean? just Tracheoesophageal fistula (HP:0002575)???
23 > id_signe_55420			Antenatal exposure : sedatives			?
24 > id_signe_29420			Storage liver disease			this is not a feature its a diagnosis!
25 > id_signe_27420			Mucous stools/acholic stools		sdoelken	? probinson?
26 > id_signe_4100			Fragility of the eye globe			?
27 > id_signe_38640			Bladder/vesical lesions/glomerulations/petechiae			? what does this mean and include?
28 > id_signe_27150			Eructation/aerophagia		sdoelken	? do we really need this?
29 > id_signe_27660			Intestinal perforation		sdoelken	do we need this? seems to be something aquired
30 > id_signe_35570			Vein of Galien dilatation/dilation		sdoelken	"I actually had to look this up - we do not use this term in german - according to wikipedia there is more than one vein named after Galen - which one are we talking about? I presume one of the cerebral ones that are nam,ed ""VEin of GAlen""? And do we really need terms for such a specific vein dilation?"
31 > id_signe_38160			Interstitial nephropathy		"skoehler, sdoelken"	"??? we have to get some more features for the histological kidney stuff into HPO - at the moment we have: Tubulointerstitial nephropathy(HP:0008654)
32 > id_signe_24760			Abnormal implantation of hair		sdoelken	? implantation?
33 > id_signe_35720			Acute ischemic syndrome		sdoelken	ischemic as in veins of leg or as in stroke like (cerebral)?
34 > id_signe_43260			Dystonia/torticollis/writer's cramp/blepharospasms		sdoelken	we have Torticollis HP:0000473; Dystonia HP:0001332 and  Blepharospasm HP:0000643 - what to do? Can orphanet go through their annotations and correct those by using the precise HPO terms for these phenotypes?
35 > id_signe_23490			Cutaneous inflammation		sdoelken	do we need this term? its very imprecise and non-informative
36 > id_signe_27240			Gastroesophageal reflux/pyrosis/esophagitis/hiatal hernia/gastroparesia		"skoehler, sdoelken"	"Gastroesophageal reflux(HP:0002020)
37 > id_signe_55300			Antenatal exposure : influenza		sdoelken	?
38 > id_signe_32600			Ground-glass/reticular/alveolar/interstitial lung/pulmonary opacity		sdoelken	?
39 > id_signe_26200			Megaesophagus/cardiospasm/congenital dilation of the esophagus/achalasia		sdoelken	? very mixed compound term
40 > id_signe_3800			Claudication/pain on mastication/while chewing		sdoelken	? probinson?
41 > id_signe_35750			Acute ischemia of the lower limbs		sdoelken	do we need this?
42 > id_signe_39580			Spermatocele/epididymal/funicular/spermatic/vaginal/albugineal cyst		sdoelken	? to many terms in one
43 > id_signe_53450			Failure to thrive/difficulties for feeding in infancy/growth delay		sdoelken	"we have Failure to thrive HP:0001508 and Feeding difficulties HP:0002022 which are in totally different sections of the HP, the first is a growth abn. the second a gastrointestinal abn"
44 > id_signe_3600			Hypoplastic maxillary bones/zygomatic bones/maxillary hypoplasia		"skoehler, sdoelken"	we have Hypoplasia of the zygomatic bone HP:0010669 and Hypoplasia of the maxilla HP:0000327 -  Can orphanet go through their annotations and correct those by using the precise HPO terms for these phenotypes?
45 > id_signe_23480			Dermal/subcutaneous infiltration/induration		sdoelken	?
46 > id_signe_26460			Intestinal atresia/stenosis/absence/agenesis/hypoplasia (excludes duodenum)		sdoelken	? excludes again...
47 > id_signe_23070			Freezing lesions		sdoelken	this is not a phenotype we want to include in HP lesions due to freezing are purely secondary phenotypes
48 > id_signe_54840			Angioedema/angioneurotic edema	Angioedema	sdoelken	# good mapping (cretaed new HP term)
49 > id_signe_55700			Monozygotic twinning		sdoelken	? I don not think we want this kind of term...
50 > id_signe_50070			Oropharyngeal neoplasm/tumor/carcinoma/cancer		sdoelken	"this is tricky - Neoplasia of the pharynx HP:0100638 belongs to Neoplasia of the respiratory system HP:0100606 and Neoplasia of the oral cavity HP:0100649 is a separat child of the parent term ""Neoplasia"" HP:0002664 - I do not think it is wise to group oral and pharynx, it seems rather random, is there a reason why not larynx...?"
51 > id_signe_54000			Health status anomalies		sdoelken	? as in immunologic - recurrent infections or something like that?
52 > id_signe_28550			Supernumerary liver/midline liver/liver/hepatic transposition		sdoelken	probinson?
53 > id_signe_55360			Antenatal exposure : ionizing radiations		sdoelken	probinson?
54 > id_signe_18480			Ectromelia/absence of one or more limb segments		sdoelken	does this refer to ectrodactyly???
55 > id_signe_52420			Total/partial monosomy/deletion		sdoelken	no phenotype  - genotype
56 > id_signe_23030			Unusual body odour		sdoelken	probinson?
57 > id_signe_22580			Dorsiflexed great toe		sdoelken	does this really occur?
58 > id_signe_26680			Short bowel		sdoelken	"short bowel syndrome as in post-operative? this would then not be a ""feature"" as such"
59 > id_signe_55380			Antenatal exposure : chemical product		sdoelken	probinson
60 > id_signe_3240			Sharp-shaped face		sdoelken	???
61 > id_signe_26400			Congenital wallet stomach/pseudo hour-glass stomach		sdoelken	probinson?
62 > id_signe_52600			Fragile chromosomal site (other than Xq28)		sdoelken	???
63 > id_signe_55320			Antenatal exposure : AIDS		sdoelken	probinson
64 > id_signe_23000			"Anomalies of skin, subcutaneous tissue and mucosae"		sdoelken	probinson?
65 > id_signe_52660			Fragile chromosome X site			probinson
66 > id_signe_24920			Scalp cyst/giant nevus		sdoelken	???
67 > id_signe_55340			Antenatal exposure : varicella		sdoelken	probinson
68 > id_signe_53000			Build/stature/longevity anomalies		sdoelken	???
69 > id_signe_52480			Insterstitial/subtelomeric microdeletion/deletion		sdoelken	probinson
70 > id_signe_20380			Thick/dowel fingers		sdoelken	???
71 > id_signe_54210			Thirst		sdoelken	probinson
72 > id_signe_49340			Organic acid metabolism anomalies		sdoelken	???
73 > id_signe_43430			Hyperesthesia/allodynia/hyperalgia		sdoelken	probinson?
74 > id_signe_20340			Spindle shaped fingers		sdoelken	???
75 > id_signe_55580			Antenatal exposure : antimiototics		sdoelken	probinson
76 > id_signe_43400			Sensitive trouble/deficit		sdoelken	?
77 > id_signe_55280			Antenatal exposure : hepatitis		sdoelken	probinson
78 > id_signe_44600			Muscular sclerosis		sdoelken	probinson
79 > id_signe_23710			Cutaneous neurofibromas/facial angiofibromas/Koenen tumors		sdoelken	too many things mixed together
80 > id_signe_55560			Antenatal exposure : cocaine/LSD		sdoelken	probinson
81 > id_signe_23740			Pedunculated skin lesions		sdoelken	probinson?
82 > id_signe_4260			Iris melanosis/ocular melanosis		sdoelken	?
83 > id_signe_55540			Antenatal exposure : alcohol		sdoelken	probinson
84 > id_signe_43180			Sphincter dysfunction		sdoelken	which sphincter???
85 > id_signe_55740			Conjoined twinning		sdoelken	probinson
86 > id_signe_43190			Motor deficit/trouble		sdoelken	"does this mean motor coordination, muscle weakness or motor delayed development?"
87 > id_signe_55520			Antenatal exposure : hormones		sdoelken	probinson
88 > id_signe_16000			"Anomalies of spine, vertebrae and pelvis"		sdoelken	pelvis is not even axial sceleton so this is really hard
89 > id_signe_26700			Short colon		sdoelken	due to operation?
90 > id_signe_8840			Nasal chondritis/nose chondritis		sdoelken	probinson?
91 > id_signe_55720			Dizygotic twinning		sdoelken	probinson?
92 > id_signe_46760			Sprain/twisted joint		sdoelken	probinson?
93 > id_signe_45510			Fibromatosis/bone fibroma		sdoelken	probinson?
94 > id_signe_25750			Punctate nails		sdoelken	?
95 > id_signe_55500			Antenatal exposure : insuline		sdoelken	probinson
96 > id_signe_49500			Lipidosis/sulfatidosis		sdoelken	probinson?
97 > id_signe_20160			Claw hand/retracted fingers		sdoelken	retracted???
98 > id_signe_50010			Head and neck neoplasm/tumor/carcinoma/cancer		sdoelken	probinson?
99 > id_signe_45930			Enlarged diaphysis/diaphyses		sdoelken	as in thickening ? long or broad???
100 > id_signe_7550			Lagophthalmia/partial palpebral occlusion		sdoelken	probinson?
101 > id_signe_40540			Dyspareunia/coital pain/vaginal dryness
102 > id_signe_40900			Penile induration
103 > id_signe_33400			Cough			rather unspecific as to the cause (lung? upper airways? gastric?)
104 > id_signe_26340			Gastric duplication		sdoelken	probinson
105 > id_signe_55260			Antenatal exposure : rubella		sdoelken	probinson
106 > id_signe_23330			Negative Nikolski's sign		sdoelken	"this is ""normal"" - so why make it a feature?"
107 > id_signe_52720			Genomic imprinting anomaly		sdoelken	probinson
108 > id_signe_55240			Antenatal exposure : syphilis		sdoelken	probinson
109 > id_signe_24400			Dense scalp hair		sdoelken	is this an abnormality???
110 > id_signe_23150			Rippled skin		sdoelken 	???
111 > id_signe_52000			Chromosomal or genetic anomaly		sdoelken	probinson
112 > id_signe_55220			Antenatal exposure : cytomegalovirus		sdoelken	probinson
113 > id_signe_55200			Antenatal exposure : toxoplasmosis		sdoelken 	probinson
114 > id_signe_3560			High cheek bones		sdoelken 	is this an abnormality?
signs: 1530
mapped: 1416
nonmapped: 114
% 92.55
...done
Start iterating the 2681 Orphanet entries.
processing orphanet number: 261102 ...  .. annotations: 8
processing orphanet number: 2793 ...  .. annotations: 12
adding alternatives:[Otoonychoperoneal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2793]
processing orphanet number: 2792 ...  .. annotations: 22
processing orphanet number: 289916 ...  .. annotations: 20
adding alternatives:[Vitamin B12-unresponsive methylmalonic acidemia, Vitamin B12-unresponsive methylmalonic aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=27, Vitamin B12-unresponsive methylmalonic acidemia type mut0, Complete deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut0, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=289916, Vitamin B12-unresponsive methylmalonic acidemia type mut-, Partial deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut-, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79312]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1461 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2791 ...  .. annotations: 25
adding alternatives:[Otodental syndrome, Globodontia, Otodental dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2791, Oculootodental syndrome, OOD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99806]
processing orphanet number: 2790 ...  .. annotations: 14
adding alternatives:[Autosomal dominant osteosclerosis, Worth type, Endosteal hyperostosis, Worth type, Worth syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2790]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 2306 ...  .. annotations: 17
adding alternatives:[Isotretinoin-like syndrome, Kawashima syndrome, Microtia-aortic arch syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2306]
processing orphanet number: 1459 ...  .. annotations: 9
adding alternatives:[Celiac disease, epilepsy and cerebral calcification syndrome, CEC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1459]
processing orphanet number: 1458 ...  .. annotations: 32
adding alternatives:[CODAS syndrome, Cerebro-oculo-dento-auriculo-skeletal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1458]
processing orphanet number: 2305 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 2789 ...  .. annotations: 42
adding alternatives:[Lateral meningocele syndrome, Lehman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2789]
processing orphanet number: 31112 ...  .. annotations: 6
NO OMIMENTRY FOR OMIM-ID 607907 creating NEW one
processing orphanet number: 52055 ...  .. annotations: 23
adding alternatives:[Agenesis of the corpus callosum-intellectual disability-coloboma-micrognathia syndrome, Graham-Cox syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52055]
processing orphanet number: 2788 ...  .. annotations: 21
adding alternatives:[Osteoporosis - pseudoglioma, OPPG, Ocular form of osteogenesis imperfecta, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2788]
processing orphanet number: 2787 ...  .. annotations: 11
processing orphanet number: 1455 ...  .. annotations: 6
processing orphanet number: 2785 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2301 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 1454 ...  .. annotations: 49
adding alternatives:[Joubert syndrome with hepatic defect, COACH syndrome, Cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis, Gentile syndrome, JS-H, Joubert syndrome with congenital hepatic fibrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1454]
processing orphanet number: 2300 ...  .. annotations: 5
adding alternatives:[Multiple intestinal atresia, Familial intestinal polyatresia syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2300, Combined immunodeficiency-enteropathy spectrum, CID-MIA/early-onset IBD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=436252]
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 1453 ...  .. annotations: 9
adding alternatives:[Cleidorhizomelic syndrome, Rhizomelic shortness with clavicular defect, Wallis-Zieff-Goldblatt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1453]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 52056 ...  .. annotations: 11
adding alternatives:[Ulnar/fibula ray defect - brachydactyly, Morava-Mehes syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52056]
processing orphanet number: 1452 ...  .. annotations: 40
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 230839 ...  .. annotations: 21
adding alternatives:[Ehlers-Danlos syndrome due to tenascin-X deficiency, EDS, classic-like type, Ehlers-Danlos syndrome, classic-like type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=230839]
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90318 ...  .. annotations: 24
adding alternatives:[Ehlers-Danlos syndrome, classic type, EDS, classic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=287, Ehlers-Danlos syndrome type 2, EDS II, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90318]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2309 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2308 ...  .. annotations: 75
adding alternatives:[Jacobsen syndrome, Del(11)(q23.3), Del(11)(qter), Distal deletion 11q, Distal monosomy 11q, Monosomy 11qter, Telomeric deletion 11q, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2308]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 2307 ...  .. annotations: 18
adding alternatives:[IVIC syndrome, Oculo-oto-radial syndrome, Radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2307]
processing orphanet number: 69735 ...  .. annotations: 18
adding alternatives:[Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome, Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69735]
processing orphanet number: 90797 ...  .. annotations: 9
adding alternatives:[Partial androgen insensitivity syndrome, PAIS, Partial androgen resistance syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90797]
processing orphanet number: 1473 ...  .. annotations: 18
adding alternatives:[Uveal coloboma-cleft lip and palate-intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1473]
processing orphanet number: 1471 ...  .. annotations: 10
adding alternatives:[Coloboma of macula - brachydactyly type B, Sorsby syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1471]
processing orphanet number: 2316 ...  .. annotations: 30
adding alternatives:[Johnson neuroectodermal syndrome, Alopecia-anosmia-deafness-hypogonadism syndrome, Johnson-McMillin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2316]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2315 ...  .. annotations: 35
adding alternatives:[Johanson-Blizzard syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2315]
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 56425 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2314 ...  .. annotations: 38
adding alternatives:[Autosomal dominant hyper-IgE syndrome, AD-HIES, Autosomal dominant HIES, Autosomal dominant hyperimmunoglobulin E syndrome, Buckley syndrome, Hyperimmunoglobulin E syndrome type 1, Hyperimmunoglobulin E-recurrent infection syndrome, Job syndrome, STAT3 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2314]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 2798 ...  .. annotations: 3
adding alternatives:[Pachygyria - intellectual disability - epilepsy, Kuzniecky syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2798]
processing orphanet number: 1467 ...  .. annotations: 70
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 1466 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1465 ...  .. annotations: 54
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 2796 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 54247 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 2311 ...  .. annotations: 38
processing orphanet number: 6 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2795 ...  .. annotations: 5
processing orphanet number: 7 ...  .. annotations: 64
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2310 ...  .. annotations: 9
adding alternatives:[Absence deformity of leg - cataract, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2310]
processing orphanet number: 9 ...  .. annotations: 16
processing orphanet number: 44890 ...  .. annotations: 18
adding alternatives:[Gastrointestinal stromal tumor, GIST, Gastrointestinal stromal sarcoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=44890]
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90307 ...  .. annotations: 14
NO OMIMENTRY FOR OMIM-ID 608355 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 90309 ...  .. annotations: 29
adding alternatives:[Ehlers-Danlos syndrome, classic type, EDS, classic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=287, Ehlers-Danlos syndrome type 1, EDS I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90309]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 90308 ...  .. annotations: 32
adding alternatives:[Angioosteohypertrophic syndrome, Klippel-Trénaunay-Weber syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2346, Klippel-Trénaunay syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90308]
processing orphanet number: 2319 ...  .. annotations: 29
adding alternatives:[Juberg-Hayward syndrome, Cleft lip/palate - abnormal thumbs - microcephaly, Orocraniodigital syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2319]
processing orphanet number: 2318 ...  .. annotations: 33
processing orphanet number: 163937 ...  .. annotations: 25
adding alternatives:[X-linked intellectual disability, Najm type, MICPCH, X-linked intellectual disability - microcephaly - pontocerebellar hypoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163937]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 90340 ...  .. annotations: 43
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90340]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 90342 ...  .. annotations: 10
adding alternatives:[Xeroderma pigmentosum, XP, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=910, Xeroderma pigmentosum variant, XPV, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90342]
processing orphanet number: 1000 ...  .. annotations: 8
adding alternatives:[Ocular albinism with late-onset sensorineural deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1000]
processing orphanet number: 2331 ...  .. annotations: 40
NO OMIMENTRY FOR OMIM-ID 611775 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 1484 ...  .. annotations: 9
adding alternatives:[Contractures - ectodermal dysplasia - cleft lip/palate, Ladda-Zonana-Ramer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1484]
processing orphanet number: 2328 ...  .. annotations: 21
adding alternatives:[Kapur-Toriello syndrome, Cleft lip/palate - facial, eye, heart and intestinal anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2328]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1479 ...  .. annotations: 3
adding alternatives:[Atrial septal defect - atrioventricular conduction defects, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1479]
processing orphanet number: 2326 ...  .. annotations: 18
processing orphanet number: 1478 ...  .. annotations: 2
processing orphanet number: 2325 ...  .. annotations: 21
processing orphanet number: 2324 ...  .. annotations: 13
adding alternatives:[Kaler-Garrity-Stern syndrome, Osteopenia - intellectual disability - sparse hair, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2324]
processing orphanet number: 2323 ...  .. annotations: 37
adding alternatives:[Sanjad-Sakati syndrome, HRD syndrome, Hypoparathyroidism - intellectual disability - dysmorphism, Hypoparathyroidism - short stature - intellectual disability - seizures, Middle-East syndrome, Richadson-Kirk syndrome, SSS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2323]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2322 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1475 ...  .. annotations: 14
adding alternatives:[Renal coloboma syndrome, Coloboma of optic nerve with renal disease, Papillo-renal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1475]
processing orphanet number: 2321 ...  .. annotations: 19
adding alternatives:[Jung-Wolff-Back-Stahl syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2321]
  ... no hpo-term mapping for orphanet annotation: 24400
processing orphanet number: 2329 ...  .. annotations: 10
adding alternatives:[Karsch-Neugebauer syndrome, Split hand/split foot - nystagmus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2329]
processing orphanet number: 137658 ...  .. annotations: 26
adding alternatives:[Microcephaly - intellectual disability - phalangeal and neurological anomalies, Woods-Crouchman-Huson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=137658]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1495 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2342 ...  .. annotations: 16
adding alternatives:[Haim-Munk syndrome, Keratosis palmoplantaris - periodontopathia - onychogryposis, Palmoplantar hyperkeratosis - periodontopathia - onychogryposis, Palmoplantar keratoderma - periodontopathia - onychogryposis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2342]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 1010 ...  .. annotations: 4
adding alternatives:[Autosomal dominant palmoplantar keratoderma and congenital alopecia, Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia, PPK-CA, Stevanovic type, Palmoplantar keratoderma and congenital alopecia, Stevanovic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1010]
processing orphanet number: 1493 ...  .. annotations: 32
adding alternatives:[Vici syndrome, Dionisi-Vici-Sabetta-Gambarara syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1493]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2340 ...  .. annotations: 22
processing orphanet number: 1492 ...  .. annotations: 14
processing orphanet number: 1490 ...  .. annotations: 6
adding alternatives:[Corneal dystrophy - perceptive deafness, CDPD, Corneal dystrophy with progressive deafness, Harboyan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1490]
processing orphanet number: 98296 ...  .. annotations: 1
processing orphanet number: 39041 ...  .. annotations: 28
adding alternatives:[Omenn syndrome, Combined immunodeficiency with hypereosinophilia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=39041]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 98299 ...  .. annotations: 1
processing orphanet number: 1008 ...  .. annotations: 17
adding alternatives:[Alopecia-epilepsy-pyorrhea-intellectual disability syndrome, Shokeir syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1008]
processing orphanet number: 2339 ...  .. annotations: 9
adding alternatives:[Keratosis follicularis - dwarfism - cerebral atrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2339]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 98293 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 2338 ...  .. annotations: 11
processing orphanet number: 98292 ...  .. annotations: 28
adding alternatives:[Maculopapular cutaneous mastocytosis, Urticaria pigmentosa, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79457, Mastocytosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98292]
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 1006 ...  .. annotations: 12
processing orphanet number: 2337 ...  .. annotations: 8
adding alternatives:[Non-epidermolytic palmoplantar keratoderma, Autosomal dominant diffuse palmoplantar keratoderma, Norrbotten type, NEPPK, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2337]
processing orphanet number: 1005 ...  .. annotations: 35
adding alternatives:[Alopecia-contractures-dwarfism-intellectual disability syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1005]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1488 ...  .. annotations: 27
adding alternatives:[Cooper-Jabs syndrome, Aural atresia - multiple congenital anomalies - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1488]
processing orphanet number: 2335 ...  .. annotations: 27
processing orphanet number: 1003 ...  .. annotations: 5
adding alternatives:[Scalp defects - postaxial polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1003]
processing orphanet number: 1487 ...  .. annotations: 10
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1487]
processing orphanet number: 1486 ...  .. annotations: 20
adding alternatives:[Lethal congenital contracture syndrome type 1, Herva disease, LCCS1, Multiple contracture syndrome, Finnish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1486]
processing orphanet number: 2333 ...  .. annotations: 27
processing orphanet number: 1002 ...  .. annotations: 21
processing orphanet number: 1001 ...  .. annotations: 52
adding alternatives:[2q37 microdeletion syndrome, Albright hereditary osteodystrophy type 3, Albright hereditary osteodystrophy-like syndrome, Brachydactyly-intellectual disability, Del(2)(q37), Deletion 2q37, Deletion 2q37-qter, Monosomy 2q37-qter, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1001]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2332 ...  .. annotations: 31
adding alternatives:[KBG syndrome, Short stature - facial and skeletal anomalies - intellectual disability - macrodontia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2332]
processing orphanet number: 1485 ...  .. annotations: 8
adding alternatives:[Arthrogryposis - hyperkeratosis, lethal form, Johnston-Aarons-Schelley syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1485]
processing orphanet number: 90363 ...  .. annotations: 16
processing orphanet number: 90362 ...  .. annotations: 28
adding alternatives:[Primary intestinal lymphangiectasia, Waldmann disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90362]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 261144 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2353 ...  .. annotations: 32
adding alternatives:[Schilbach-Rott syndrome, BRSS, Hypotelorism - cleft palate - hypospadias, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2353]
processing orphanet number: 3200 ...  .. annotations: 21
processing orphanet number: 1021 ...  .. annotations: 11
adding alternatives:[Amaurosis-hypertrichosis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1021]
processing orphanet number: 2352 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 55720
processing orphanet number: 2351 ...  .. annotations: 11
processing orphanet number: 57782 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 45510
processing orphanet number: 276630 ...  .. annotations: 20
processing orphanet number: 2349 ...  .. annotations: 15
processing orphanet number: 2348 ...  .. annotations: 36
adding alternatives:[Familial partial lipodystrophy, Dunnigan type, Dunnigan syndrome, FPLD2, Familial partial lipodystrophy type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2348]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 2347 ...  .. annotations: 30
adding alternatives:[Lethal Kniest-like dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2347]
processing orphanet number: 2346 ...  .. annotations: 43
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 28378 ...  .. annotations: 21
adding alternatives:[Tyrosinemia type 2, Keratosis palmoplantaris - corneal dystrophy, Oculocutaneous tyrosinemia, Richner-Hanhart syndrome, Tyrosinemia due to TAT deficiency, Tyrosinemia due to tyrosine aminotransferase deficiency, Tyrosinemia type II, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=28378]
processing orphanet number: 1014 ...  .. annotations: 4
adding alternatives:[Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome, Devriendt-Vandenberghe-Fryns syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1014]
processing orphanet number: 2345 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 1497 ...  .. annotations: 8
adding alternatives:[X-linked complicated corpus callosum dysgenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1497, L1 syndrome, CRASH syndrome, Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome, L1CAM syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=275543]
processing orphanet number: 1496 ...  .. annotations: 14
adding alternatives:[Corpus callosum agenesis - neuronopathy, Andermann syndrome, Charlevoix disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1496]
processing orphanet number: 2343 ...  .. annotations: 14
processing orphanet number: 231720 ...  .. annotations: 5
adding alternatives:[Non-acquired combined pituitary hormone deficiency with spine abnormalities, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231720]
processing orphanet number: 90354 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2363 ...  .. annotations: 52
adding alternatives:[Lacrimoauriculodentodigital syndrome, LADD syndrome, LARD syndrome, Lacrimoauriculoradiodental syndrome, Levy-Hollister syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2363]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3210 ...  .. annotations: 23
adding alternatives:[Summitt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3210]
processing orphanet number: 1031 ...  .. annotations: 7
adding alternatives:[Amelogenesis imperfecta-nephrocalcinosis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1031]
processing orphanet number: 90350 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3207 ...  .. annotations: 16
processing orphanet number: 1028 ...  .. annotations: 15
adding alternatives:[Amelo-onycho-hypohidrotic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1028]
processing orphanet number: 3206 ...  .. annotations: 37
adding alternatives:[Stüve-Wiedemann syndrome, Stüve-Wiedemann dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3206]
processing orphanet number: 3205 ...  .. annotations: 30
adding alternatives:[Sturge-Weber syndrome, Encephalofacial angiomatosis, Encephalotrigeminal angiomatosis, SWS, Sturge-Weber-Dimitri syndrome, Sturge-Weber-Krabbe angiomatosis, Sturge-Weber-Krabbe syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3205]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 1027 ...  .. annotations: 12
adding alternatives:[Autosomal recessive amelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1027]
processing orphanet number: 3204 ...  .. annotations: 13
adding alternatives:[Stormorken-Sjaastad-Langslet syndrome, Thrombocytopathy - asplenia - miosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3204]
processing orphanet number: 3201 ...  .. annotations: 20
adding alternatives:[Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence, Stoll-Kieny-Dott syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3201]
processing orphanet number: 90349 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 603 ...  .. annotations: 2
adding alternatives:[Distal myopathy, Welander type, WDM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=603]
processing orphanet number: 90348 ...  .. annotations: 14
processing orphanet number: 606 ...  .. annotations: 3
adding alternatives:[Proximal myotonic myopathy, Myotonic dystrophy type 2, Proximal myotonic dystrophy, Ricker disease, Ricker syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=606]
processing orphanet number: 261120 ...  .. annotations: 24
adding alternatives:[14q11.2 microdeletion syndrome, Del(14)(q11.2), Monosomy 14q11.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261120]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 157215 ...  .. annotations: 7
adding alternatives:[Hereditary hypophosphatemic rickets with hypercalciuria, HHRH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157215]
processing orphanet number: 42665 ...  .. annotations: 7
adding alternatives:[Tietz syndrome, Hypopigmentation-deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=42665]
processing orphanet number: 2375 ...  .. annotations: 14
adding alternatives:[Laryngeal abductor paralysis - intellectual disability, Plott syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2375]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3222 ...  .. annotations: 15
adding alternatives:[Phosphoribosylpyrophosphate synthetase superactivity, PRPP synthetase superactivity, PRPS1 superactivity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3222]
processing orphanet number: 2374 ...  .. annotations: 7
adding alternatives:[Congenital laryngeal web, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2374]
processing orphanet number: 3221 ...  .. annotations: 8
processing orphanet number: 29207 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 2373 ...  .. annotations: 5
adding alternatives:[Congenital laryngomalacia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2373]
processing orphanet number: 3220 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 1041 ...  .. annotations: 1
adding alternatives:[Hb Bart's hydrops fetalis, Alpha-thalassemia hydrops fetalis, Alpha-thalassemia major, Hemoglobin Bart's hydrops fetalis, Homozygous alpha0-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163596, Hydrops fetalis, Fetal anasarca, Fetal hydrops, Generalized fetal edema, HF, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1041, Non-immune hydrops fetalis, Non-immune HF, Non-immune fetal edema, Non-immune fetal hydrops, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=363999]
processing orphanet number: 1040 ...  .. annotations: 10
processing orphanet number: 137608 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 2371 ...  .. annotations: 24
adding alternatives:[Lethal Larsen-like syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2371]
processing orphanet number: 2370 ...  .. annotations: 22
adding alternatives:[Larsen-like osseous dysplasia - short stature, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2370]
processing orphanet number: 3219 ...  .. annotations: 37
adding alternatives:[Fountain syndrome, Deafness - skeletal dysplasia - coarse face with full lips, Deafness - skeletal dysplasia - lip granuloma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3219]
processing orphanet number: 79113 ...  .. annotations: 29
adding alternatives:[Mandibulofacial dysostosis-microcephaly syndrome, Growth delay - intellectual disability - mandibulofacial dysostosis - microcephaly - cleft palate, MFDM syndrome, Mandibulofacial dysostosis, Guion-Almeida type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79113]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3218 ...  .. annotations: 20
adding alternatives:[Deafness - epiphyseal dysplasia - short stature, Chitty-Hall-Baraitser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3218]
processing orphanet number: 3217 ...  .. annotations: 14
adding alternatives:[Deafness -  small bowel diverticulosis - neuropathy, Groll-Hirschowitz syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3217]
processing orphanet number: 2369 ...  .. annotations: 22
processing orphanet number: 3216 ...  .. annotations: 14
adding alternatives:[Conductive deafness - malformed external ear, Mengel-Konigsmark syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3216]
processing orphanet number: 2368 ...  .. annotations: 3
adding alternatives:[Gastroschisis, Laparoschisis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2368]
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 1037 ...  .. annotations: 14
processing orphanet number: 610 ...  .. annotations: 7
processing orphanet number: 3214 ...  .. annotations: 23
adding alternatives:[Deaf blind hypopigmentation syndrome, Yemenite type, Warburg-Thomsen syndrome, Yemenite deaf-blind hypopigmentation syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3214]
processing orphanet number: 611 ...  .. annotations: 8
adding alternatives:[Inclusion body myositis, IBM, Sporadic inclusion body myositis, sIBM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=611]
processing orphanet number: 1035 ...  .. annotations: 26
adding alternatives:[Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria, Ampola syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1035]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 612 ...  .. annotations: 17
adding alternatives:[Potassium-aggravated myotonia, K+-aggravated myotonia, K-aggravated myotonia, PAM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=612, Myotonia fluctuans, Exercise-induced delayed-onset myotonia, Fluctuating myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99734, Myotonia permanens, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99735, Acetazolamide-responsive myotonia, ACZ-responsive congenital myotonia, ACZ-responsive myotonia, Acetazolamide-responsive congenital myotonia, Myotonia - painful contractions, Painful congenital myotonia, Painful myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99736]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1034 ...  .. annotations: 10
processing orphanet number: 93409 ...  .. annotations: 7
NO OMIMENTRY FOR OMIM-ID 610713 creating NEW one
processing orphanet number: 614 ...  .. annotations: 3
processing orphanet number: 93406 ...  .. annotations: 8
adding alternatives:[Syndactyly type 5, Postaxial syndactyly with metacarpal synostosis, SD5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93406]
processing orphanet number: 617 ...  .. annotations: 10
processing orphanet number: 618 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 93405 ...  .. annotations: 10
adding alternatives:[Syndactyly type 4, Polysyndactyly, Haas type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93405]
processing orphanet number: 93404 ...  .. annotations: 4
adding alternatives:[Syndactyly type 3, SD3, Syndactyly of fingers 4 and 5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93404]
processing orphanet number: 93403 ...  .. annotations: 13
processing orphanet number: 261112 ...  .. annotations: 57
adding alternatives:[Monosomy 9p, 9p deletion syndrome, 9p- syndrome, Alfi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261112]
  ... no hpo-term mapping for orphanet annotation: 52420
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 93402 ...  .. annotations: 4
processing orphanet number: 1055 ...  .. annotations: 1
processing orphanet number: 2386 ...  .. annotations: 6
processing orphanet number: 3233 ...  .. annotations: 5
adding alternatives:[Cochleosaccular degeneration - cataract, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3233]
processing orphanet number: 3232 ...  .. annotations: 9
adding alternatives:[Deafness - ear malformation - facial palsy, Sellars-Beighton syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3232]
processing orphanet number: 1053 ...  .. annotations: 3
processing orphanet number: 3231 ...  .. annotations: 49
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 293168 ...  .. annotations: 10
adding alternatives:[Infantile-onset ascending hereditary spastic paralysis, IAHSP, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=293168]
processing orphanet number: 1052 ...  .. annotations: 63
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3230 ...  .. annotations: 5
adding alternatives:[Deafness - oligodontia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3230]
processing orphanet number: 1051 ...  .. annotations: 21
adding alternatives:[Ramos-Arroyo syndrome, Corneal anesthesia - deafness - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1051]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2380 ...  .. annotations: 9
adding alternatives:[Legg-Calvé-Perthes disease, Aseptic necrosis of the capital femoral epiphysis, Osteochondritis of the capital femoral epiphysis, Osteochondrosis of the capital femoral epiphysis, Perthes disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2380]
processing orphanet number: 231736 ...  .. annotations: 7
processing orphanet number: 2379 ...  .. annotations: 9
adding alternatives:[Early-onset parkinsonism - intellectual disability, Laxova-Opitz syndrome, Waisman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2379]
processing orphanet number: 3226 ...  .. annotations: 29
adding alternatives:[Deafness - lymphedema - leukemia, Emberger syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3226]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1048 ...  .. annotations: 4
adding alternatives:[Isolated anencephaly/exencephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1048]
processing orphanet number: 2378 ...  .. annotations: 26
adding alternatives:[Laurin-Sandrow syndrome, Mirror hands and feets - nasal defects, Sandrow syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2378]
processing orphanet number: 3225 ...  .. annotations: 3
processing orphanet number: 1046 ...  .. annotations: 22
adding alternatives:[Lethal hemolytic anemia - genital anomalies, Water-West syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1046]
processing orphanet number: 2377 ...  .. annotations: 26
adding alternatives:[Laurence-Moon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2377]
processing orphanet number: 3224 ...  .. annotations: 27
processing orphanet number: 622 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79107 ...  .. annotations: 22
adding alternatives:[Developmental malformations - deafness - dystonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79107]
  ... no hpo-term mapping for orphanet annotation: 26200
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 624 ...  .. annotations: 25
adding alternatives:[Familial multiple nevi flammei, Familial multiple port-wine stains, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=624]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 626 ...  .. annotations: 14
adding alternatives:[Large congenital melanocytic nevus, Congenital pigmented nevus, GMN, Giant congenital melanocytic nevus, Giant pigmented hairy nevus, LCMN, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=626]
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 627 ...  .. annotations: 18
adding alternatives:[Nance-Horan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=627]
processing orphanet number: 628 ...  .. annotations: 45
adding alternatives:[Diastrophic dwarfism, Diastrophic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=628]
processing orphanet number: 139406 ...  .. annotations: 11
adding alternatives:[Encephalopathy due to prosaposin deficiency, Combined prosaposin deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139406]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1065 ...  .. annotations: 10
adding alternatives:[Aniridia-cerebellar ataxia-intellectual disability syndrome, Gillespie syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1065]
processing orphanet number: 2396 ...  .. annotations: 32
adding alternatives:[Encephalocraniocutaneous lipomatosis, Haberland syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2396]
processing orphanet number: 3243 ...  .. annotations: 33
NO OMIMENTRY FOR OMIM-ID 608068 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 1064 ...  .. annotations: 17
adding alternatives:[Aniridia - renal agenesis - psychomotor retardation, Sommer-Rathbun-Battles syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1064]
processing orphanet number: 3242 ...  .. annotations: 47
adding alternatives:[Renpenning syndrome, X-linked intellectual disability due to PQBP1 mutations, X-linked intellectual disability, Renpenning type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3242]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3241 ...  .. annotations: 15
adding alternatives:[Deafness-craniofacial syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3241]
processing orphanet number: 2394 ...  .. annotations: 11
adding alternatives:[Pyruvate dehydrogenase deficiency, PDH, PDHC, Pyruvate dehydrogenase complex deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=765, Pyruvate dehydrogenase E3 deficiency, DLD deficiency, Dihydrolipoamide dehydrogenase deficiency, E3-deficient maple syrup urine disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2394]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 75563 ...  .. annotations: 10
adding alternatives:[X-linked sideroblastic anemia, XLSA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75563]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 1062 ...  .. annotations: 4
adding alternatives:[Hereditary neurocutaneous angioma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1062]
processing orphanet number: 3240 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2391 ...  .. annotations: 4
adding alternatives:[Congenitally short costocoracoid ligament, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2391]
processing orphanet number: 2390 ...  .. annotations: 14
adding alternatives:[Lichstenstein syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2390]
  ... no hpo-term mapping for orphanet annotation: 55260
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 3239 ...  .. annotations: 7
adding alternatives:[Deafness - vitiligo - achalasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3239]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 3238 ...  .. annotations: 9
adding alternatives:[Cardiospondylocarpofacial syndrome, Forney syndrome, Forney-Robinson-Pascoe syndrome, Mitral regurgitation - deafness - skeletal anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3238]
processing orphanet number: 631 ...  .. annotations: 4
processing orphanet number: 1059 ...  .. annotations: 15
adding alternatives:[Blue rubber bleb nevus, Bean syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1059]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 3237 ...  .. annotations: 10
processing orphanet number: 3236 ...  .. annotations: 18
adding alternatives:[Conductive deafness - ptosis - skeletal anomalies, Jackson-Barr syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3236]
processing orphanet number: 2388 ...  .. annotations: 59
adding alternatives:[Choreoacanthocytosis, ChAc, Chorea-acanthocytosis, Levine-Critchley syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2388]
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 43500
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 633 ...  .. annotations: 31
adding alternatives:[Laron syndrome, Complete growth hormone insensitivity, GH receptor deficiency, Growth hormone receptor deficiency, Laron-type dwarfism, Primary GH insensitivity, Primary GH resistance, Primary growth hormone insensitivity, Primary growth hormone resistance, Short stature due to growth hormone resistance, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=633]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 634 ...  .. annotations: 28
adding alternatives:[Netherton syndrome, Bamboo hair syndrome, Comèl-Netherton syndrome, NS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=634]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2387 ...  .. annotations: 10
adding alternatives:[Leukonychia totalis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2387]
processing orphanet number: 635 ...  .. annotations: 3
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 636 ...  .. annotations: 50
  ... no hpo-term mapping for orphanet annotation: 23710
processing orphanet number: 261190 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 637 ...  .. annotations: 25
adding alternatives:[Neurofibromatosis type 2, Familial acoustic neurinoma, Familial acoustic neuroma, Familial vestibular schwannoma, NF2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=637]
  ... no hpo-term mapping for orphanet annotation: 23710
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 638 ...  .. annotations: 18
adding alternatives:[Neurofibromatosis-Noonan syndrome, NFNS, Neurofibromatosis type 1-Noonan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=638]
processing orphanet number: 139411 ...  .. annotations: 21
NO OMIMENTRY FOR OMIM-ID 604287 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 264200 ...  .. annotations: 33
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2055, 14q22q23 microdeletion syndrome, 14q22-q23 microdeletion syndrome, Del(14)(q22q23), Monosomy 14q22-q23, Monosomy 14q22q23, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=264200]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1077 ...  .. annotations: 6
processing orphanet number: 3255 ...  .. annotations: 14
adding alternatives:[Filippi syndrome, Syndactyly type 1 - microcephaly - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3255]
processing orphanet number: 3253 ...  .. annotations: 41
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3253]
processing orphanet number: 1074 ...  .. annotations: 6
processing orphanet number: 66625 ...  .. annotations: 24
adding alternatives:[Cerebro-oculo-nasal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=66625]
processing orphanet number: 1072 ...  .. annotations: 6
adding alternatives:[Ankyloblepharon filiforme adnatum - cleft palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1072]
processing orphanet number: 3250 ...  .. annotations: 15
processing orphanet number: 1071 ...  .. annotations: 29
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1071]
processing orphanet number: 1070 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 54840
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 66629 ...  .. annotations: 23
adding alternatives:[Goldberg-Shprintzen megacolon syndrome, GOSHS, Megacolon - microcephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=66629]
processing orphanet number: 34217 ...  .. annotations: 14
adding alternatives:[Naxos disease, KWWH type I, Keratoderma with woolly hair type I, Keratosis palmoplantaris with arrythmogenic cardiomyopathy, Palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy, Palmoplantar keratoderma with arrythmogenic cardiomyopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=34217]
processing orphanet number: 640 ...  .. annotations: 13
adding alternatives:[Hereditary neuropathy with liability to pressure palsies, Current pressure-sensitive neuropathy, HNPP, Heterozygous microdeletion 17p11.2p12, Potato-grubbing palsy, Tomaculous neuropathy, Tulip-bulb digger's palsy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=640]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 228116 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 642 ...  .. annotations: 9
adding alternatives:[Hereditary sensory and autonomic neuropathy type 4, HSAN4, Insensitivity to pain - anhidrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=642]
processing orphanet number: 3248 ...  .. annotations: 5
adding alternatives:[Distal symphalangism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3248]
processing orphanet number: 1069 ...  .. annotations: 8
adding alternatives:[Aniridia-absent patella syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1069]
processing orphanet number: 1068 ...  .. annotations: 6
processing orphanet number: 2399 ...  .. annotations: 16
adding alternatives:[Nasopalpebral lipoma - coloboma - telecanthus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2399]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 7550
processing orphanet number: 3246 ...  .. annotations: 9
adding alternatives:[Symphalangism with multiple anomalies of hands and feet, Learman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3246]
processing orphanet number: 2398 ...  .. annotations: 10
adding alternatives:[Multiple symmetric lipomatosis, Cephalothoracic lipodystrophy, Familial benign cervical lipomatosis, Launois-Bensaude lipomatosis, Madelung disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2398]
processing orphanet number: 1067 ...  .. annotations: 13
processing orphanet number: 646 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 647 ...  .. annotations: 44
adding alternatives:[Nijmegen breakage syndrome, AT V1, Ataxia-telangiectasia, variant 1, Berlin breakage syndrome, Immunodeficiency - microcephaly - chromosomal instability, Microcephaly - immunodeficiency - lymphoreticuloma, NBS, Seemanova syndrome type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=647]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 648 ...  .. annotations: 57
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 649 ...  .. annotations: 64
adding alternatives:[Norrie disease, Atrophia bulborum hereditaria, Episkopi blindness, Norrie-Warburg disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=649]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 66630 ...  .. annotations: 5
adding alternatives:[Congenital pseudoarthrosis of clavicle, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=66630]
processing orphanet number: 66633 ...  .. annotations: 6
processing orphanet number: 66631 ...  .. annotations: 34
adding alternatives:[CEDNIK syndrome, Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=66631]
processing orphanet number: 1088 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3266 ...  .. annotations: 9
processing orphanet number: 66637 ...  .. annotations: 11
adding alternatives:[Diaphanospondylodysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=66637]
processing orphanet number: 3265 ...  .. annotations: 12
processing orphanet number: 3262 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 650 ...  .. annotations: 13
processing orphanet number: 651 ...  .. annotations: 13
processing orphanet number: 652 ...  .. annotations: 13
adding alternatives:[Multiple endocrine neoplasia type 1, MEN1, Wermer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=652]
processing orphanet number: 653 ...  .. annotations: 65
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 3259 ...  .. annotations: 3
adding alternatives:[Syndactyly-polydactyly-ear lobe syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3259]
processing orphanet number: 654 ...  .. annotations: 11
processing orphanet number: 3258 ...  .. annotations: 43
adding alternatives:[Cenani-Lenz syndrome, Cenani syndactyly, Cenani-Lenz syndactyly, Syndactyly type 7, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3258]
processing orphanet number: 33355 ...  .. annotations: 23
adding alternatives:[Reticular dysgenesis, AK2 deficiency, Congenital aleukocytosis, De Vaal disease, Generalized hematopoietic hypoplasia, SCID with leukopenia, Severe combined immunodeficiency with leukopenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33355]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 655 ...  .. annotations: 5
processing orphanet number: 1078 ...  .. annotations: 7
adding alternatives:[Thumb stiffness - brachydactyly - intellectual disability, Piussan-Lenaerts-Mathieu syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1078]
processing orphanet number: 657 ...  .. annotations: 4
processing orphanet number: 658 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 659 ...  .. annotations: 22
processing orphanet number: 252206 ...  .. annotations: 6
adding alternatives:[Melanoma and neural system tumor syndrome, Melanoma-astrocytoma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=252206]
  ... no hpo-term mapping for orphanet annotation: 23710
processing orphanet number: 139436 ...  .. annotations: 6
processing orphanet number: 98697 ...  .. annotations: 1
processing orphanet number: 3275 ...  .. annotations: 12
adding alternatives:[Spondylocarpotarsal synostosis, Synspondylism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3275]
processing orphanet number: 66646 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 1094 ...  .. annotations: 9
NO OMIMENTRY FOR OMIM-ID 607214 creating NEW one
processing orphanet number: 1092 ...  .. annotations: 23
adding alternatives:[Renal-genital-middle ear anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1092]
processing orphanet number: 3270 ...  .. annotations: 21
adding alternatives:[Radio-ulnar synostosis - intellectual disability - hypotonia, Der Kaloustian-McIntosh-Silver syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3270]
processing orphanet number: 660 ...  .. annotations: 4
processing orphanet number: 661 ...  .. annotations: 7
adding alternatives:[Ondine syndrome, CCHS, Central congenital hypoventilation syndrome, Congenital central alveolar hypoventilation syndrome, Ondine curse, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=661, Haddad syndrome, Congenital central alveolar hypoventilation - Hirschsprung disease, Ondine-Hirschsprung disease, Ondine-Hirschsprung syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99803]
processing orphanet number: 662 ...  .. annotations: 15
adding alternatives:[Yellow nail syndrome, Lymphedema with yellow nails, YNS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=662]
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 664 ...  .. annotations: 7
adding alternatives:[Ornithine transcarbamylase deficiency, OCT deficiency, OTC deficiency, Ornithine carbamoyltransferase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=664]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 665 ...  .. annotations: 33
processing orphanet number: 666 ...  .. annotations: 53
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 3268 ...  .. annotations: 18
NO OMIMENTRY FOR OMIM-ID 603438 creating NEW one
processing orphanet number: 667 ...  .. annotations: 45
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3267 ...  .. annotations: 16
adding alternatives:[Isolated cloverleaf skull syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2343, Familial lambdoid synostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3267, Isolated scaphocephaly, Isolated dolichocephaly, Non-syndromic sagittal synostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35093]
processing orphanet number: 669 ...  .. annotations: 47
processing orphanet number: 3287 ...  .. annotations: 41
adding alternatives:[Takayasu arteritis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3287]
  ... no hpo-term mapping for orphanet annotation: 35390
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 3286 ...  .. annotations: 3
processing orphanet number: 3283 ...  .. annotations: 3
processing orphanet number: 671 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 672 ...  .. annotations: 39
adding alternatives:[Pallister-Hall syndrome, Hypothalamic hamartoblastoma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=672]
processing orphanet number: 228169 ...  .. annotations: 8
adding alternatives:[Autosomal dominant striatal neurodegeneration, ADSD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228169]
processing orphanet number: 96061 ...  .. annotations: 44
processing orphanet number: 675 ...  .. annotations: 4
adding alternatives:[Annular pancreas, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=675]
processing orphanet number: 31153 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 678 ...  .. annotations: 27
adding alternatives:[Papillon-Lefèvre syndrome, Keratosis palmoplantar - periodontopathy, PLS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=678]
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 679 ...  .. annotations: 37
adding alternatives:[Malignant atrophic papulosis, Degos disease, Köhlmeier-Degos disease, Köhlmeier-Degos-Delort-Tricort syndrome, Papulosis atrophican maligna, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=679]
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 84085 ...  .. annotations: 7
processing orphanet number: 3291 ...  .. annotations: 25
NO OMIMENTRY FOR OMIM-ID 272950 creating NEW one
processing orphanet number: 66661 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 181393 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 48818 ...  .. annotations: 20
adding alternatives:[Aceruloplasminemia, Hereditary ceruloplasmin deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=48818]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 3294 ...  .. annotations: 6
adding alternatives:[Extensor tendons of finger anomalies, Hapnes-Boman-Skeie syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3294]
processing orphanet number: 3293 ...  .. annotations: 13
processing orphanet number: 3292 ...  .. annotations: 46
adding alternatives:[Tel Hashomer camptodactyly syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3292]
processing orphanet number: 682 ...  .. annotations: 30
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=682]
processing orphanet number: 52022 ...  .. annotations: 3
adding alternatives:[Potocki-Shaffer syndrome, 11p11.2 deletion, Proximal 11p deletion syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52022]
processing orphanet number: 200 ...  .. annotations: 20
processing orphanet number: 201 ...  .. annotations: 58
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 685 ...  .. annotations: 7
processing orphanet number: 202 ...  .. annotations: 13
processing orphanet number: 31142 ...  .. annotations: 7
processing orphanet number: 77301 ...  .. annotations: 24
processing orphanet number: 205 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 3289 ...  .. annotations: 2
adding alternatives:[Taurodontism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3289]
processing orphanet number: 206 ...  .. annotations: 54
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 207 ...  .. annotations: 32
adding alternatives:[Crouzon disease, Crouzon craniofacial dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=207]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 209 ...  .. annotations: 76
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 46627 ...  .. annotations: 25
adding alternatives:[Char syndrome, Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46627]
processing orphanet number: 33314 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 211 ...  .. annotations: 5
adding alternatives:[Familial cylindromatosis, Turban tumor syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=211, Brooke-Spiegler syndrome, CYLD cutaneous syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79493]
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 213 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 214 ...  .. annotations: 6
adding alternatives:[Cystinuria, Cystinuria - lysinuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=214, Cystinuria type B, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93613, Cystinuria type A, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93612]
processing orphanet number: 699 ...  .. annotations: 14
adding alternatives:[Pearson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=699]
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 216 ...  .. annotations: 17
processing orphanet number: 217 ...  .. annotations: 16
adding alternatives:[Isolated Dandy-Walker malformation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=217]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 55260
  ... no hpo-term mapping for orphanet annotation: 55300
processing orphanet number: 218 ...  .. annotations: 12
adding alternatives:[Darier disease, Darier-White disease, Keratosis follicularis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=218]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 261197 ...  .. annotations: 31
NO OMIMENTRY FOR OMIM-ID 611913 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 163966 ...  .. annotations: 26
adding alternatives:[X-linked dominant chondrodysplasia, Chassaing-Lacombe type, X-linked dominant chondrodysplasia - hydrocephaly - microphthalmia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163966]
processing orphanet number: 84090 ...  .. annotations: 10
processing orphanet number: 220 ...  .. annotations: 7
adding alternatives:[Denys-Drash syndrome, Drash syndrome, Wilms tumor and pseudohermaphroditism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=220]
processing orphanet number: 221 ...  .. annotations: 50
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 222 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 52047 ...  .. annotations: 27
adding alternatives:[Braddock syndrome, Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52047]
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 225 ...  .. annotations: 23
adding alternatives:[Maternally-inherited diabetes and deafness, MIDD, Mitochondrial diabetes, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=225]
processing orphanet number: 79501 ...  .. annotations: 8
processing orphanet number: 226 ...  .. annotations: 3
adding alternatives:[Dihydropteridine reductase deficiency, Hyperphenylalaninemia due to dihydropteridine reductase deficiency, PKU type 2, Phenylketonuria type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=226, Hyperphenylalaninemia, Hyperphenylalaninemia due to BH4 deficiency, Hyperphenylalaninemia due to tetrahydrobiopterin deficiency, Non-phenylketonuric hyperphenylalaninemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238583]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 79503 ...  .. annotations: 8
adding alternatives:[Ichthyosis hystrix of Curth-Macklin, Ichthyosis hystrix, Curth-Macklin type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79503]
processing orphanet number: 139402 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 23330
  ... no hpo-term mapping for orphanet annotation: 54840
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 79094 ...  .. annotations: 11
NO OMIMENTRY FOR OMIM-ID 602531 creating NEW one
processing orphanet number: 93393 ...  .. annotations: 3
processing orphanet number: 79095 ...  .. annotations: 14
processing orphanet number: 93396 ...  .. annotations: 6
adding alternatives:[Brachydactyly type A2, Brachydactyly, Mohr-Wriedt type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93396]
processing orphanet number: 93394 ...  .. annotations: 6
adding alternatives:[Brachydactyly type A4, Brachydactyly, Temtamy type, Brachymesophalangy II and V, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93394]
processing orphanet number: 231 ...  .. annotations: 15
processing orphanet number: 233 ...  .. annotations: 33
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 234 ...  .. annotations: 10
adding alternatives:[Dubin-Johnson syndrome, Dubin-Sprinz disease, Hyperbilirubinemia type 2, Sprinz-Nelson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=234]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 235 ...  .. annotations: 79
adding alternatives:[Dubowitz syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=235]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 236 ...  .. annotations: 25
processing orphanet number: 239 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 99927 ...  .. annotations: 8
processing orphanet number: 93389 ...  .. annotations: 13
processing orphanet number: 99928 ...  .. annotations: 9
processing orphanet number: 93388 ...  .. annotations: 13
processing orphanet number: 99925 ...  .. annotations: 7
processing orphanet number: 93387 ...  .. annotations: 8
processing orphanet number: 1909 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 1908 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 79083 ...  .. annotations: 15
adding alternatives:[PPARG-related familial partial lipodystrophy, FPLD3, Familial partial lipodystrophy type 3, PPARG-related FPLD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79083]
processing orphanet number: 79085 ...  .. annotations: 12
processing orphanet number: 79084 ...  .. annotations: 15
adding alternatives:[Familial partial lipodystrophy, Köbberling type, FPLD1, Familial partial lipodystrophy type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79084]
processing orphanet number: 79087 ...  .. annotations: 19
adding alternatives:[Partial acquired lipodystrophy, Barraquer-Simons syndrome, Progressive cephalothoracic lipodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79087]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 93385 ...  .. annotations: 3
processing orphanet number: 240 ...  .. annotations: 31
adding alternatives:[Léri-Weill dyschondrosteosis, Léri-Weill syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=240, Madelung deformity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35688]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 93384 ...  .. annotations: 11
adding alternatives:[Brachydactyly type C, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93384]
processing orphanet number: 241 ...  .. annotations: 9
processing orphanet number: 79088 ...  .. annotations: 2
processing orphanet number: 93383 ...  .. annotations: 12
adding alternatives:[Brachydactyly type B, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93383]
processing orphanet number: 242 ...  .. annotations: 5
processing orphanet number: 243 ...  .. annotations: 16
processing orphanet number: 244 ...  .. annotations: 2
processing orphanet number: 245 ...  .. annotations: 30
adding alternatives:[Nager syndrome, Mandibulofacial dysostosis with preaxial limb anomalies, NAFD, Nager acrofacial dysostosis, Preaxial acrodysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=245]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 246 ...  .. annotations: 19
adding alternatives:[Postaxial acrofacial dysostosis, Acrofacial dysostosis, Genee-Wiedmann type, Mandibulfacial dysostosis with postaxial limb anomalies, Miller syndrome, POADS, Postaxial acrodysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=246]
processing orphanet number: 248 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1906 ...  .. annotations: 9
NO OMIMENTRY FOR OMIM-ID 609442 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 55440
processing orphanet number: 1901 ...  .. annotations: 24
adding alternatives:[Ehlers-Danlos syndrome, dermatosparaxis type, EDS VIIC, Ehlers-Danlos syndrome type 7C, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1901]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 1900 ...  .. annotations: 27
adding alternatives:[Ehlers-Danlos syndrome, kyphoscoliotic type, EDS VIA, EDS, kyphoscoliotic type, EDS, oculoscoliotic type, Ehlers-Danlos syndrome type 6A, Ehlers-Danlos syndrome, oculoscoliotic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1900]
  ... no hpo-term mapping for orphanet annotation: 4100
processing orphanet number: 53715 ...  .. annotations: 23
processing orphanet number: 53719 ...  .. annotations: 24
processing orphanet number: 231393 ...  .. annotations: 7
adding alternatives:[Beta-thalassemia - X-linked thrombocytopenia, XLTT, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231393]
processing orphanet number: 1919 ...  .. annotations: 2
  ... no hpo-term mapping for orphanet annotation: 55440
processing orphanet number: 75501 ...  .. annotations: 4
adding alternatives:[Ehlers-Danlos syndrome, fibronectinemic type, EDS X, Ehlers-Danlos syndrome type 10, Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality, Ehlers-Danlos syndrome, fibronectin-deficient, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75501]
processing orphanet number: 250 ...  .. annotations: 23
processing orphanet number: 251 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 253 ...  .. annotations: 14
processing orphanet number: 1910 ...  .. annotations: 7
adding alternatives:[Fetal iodine syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1910]
processing orphanet number: 254 ...  .. annotations: 6
processing orphanet number: 255 ...  .. annotations: 4
processing orphanet number: 178509 ...  .. annotations: 14
adding alternatives:[Perry syndrome, Parkinsonism with alveolar hypoventilation and mental depression, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178509]
processing orphanet number: 85317 ...  .. annotations: 20
processing orphanet number: 256 ...  .. annotations: 7
processing orphanet number: 85318 ...  .. annotations: 5
processing orphanet number: 257 ...  .. annotations: 14
adding alternatives:[Epidermolysis bullosa simplex with muscular dystrophy, EBS-MD, Limb-girdle muscular dystrophy with epidermolysis bullosa simplex, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=257]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1918 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 1917 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 53721 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1915 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 55540
processing orphanet number: 1914 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 55480
processing orphanet number: 1913 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 55440
processing orphanet number: 1912 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 55420
  ... no hpo-term mapping for orphanet annotation: 55440
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 1911 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 55560
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 261 ...  .. annotations: 21
processing orphanet number: 262 ...  .. annotations: 14
processing orphanet number: 1920 ...  .. annotations: 23
processing orphanet number: 269 ...  .. annotations: 11
processing orphanet number: 1928 ...  .. annotations: 4
adding alternatives:[Congenital lobar emphysema, Congenital lobar hyperinflation, Infantile lobar hyperinflation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1928]
processing orphanet number: 1927 ...  .. annotations: 12
adding alternatives:[Emery-Nelson syndrome, Hand and foot deformity - flat facies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1927]
processing orphanet number: 1926 ...  .. annotations: 32
adding alternatives:[Diabetic embryopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1926]
processing orphanet number: 1923 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 55520
processing orphanet number: 99978 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 99976 ...  .. annotations: 10
adding alternatives:[Adenocarcinoma of esophagus, Esophageal adenocarcinoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99976]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99977 ...  .. annotations: 8
adding alternatives:[Squamous cell carcinoma of esophagus, ESCC, Esophageal epidermoid carcinoma, Esophageal squamous cell carcinoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99977]
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 270 ...  .. annotations: 9
adding alternatives:[Oculopharyngeal muscular dystrophy, OPMD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=270]
processing orphanet number: 99971 ...  .. annotations: 4
processing orphanet number: 273 ...  .. annotations: 23
adding alternatives:[Steinert myotonic dystrophy, DM1, MD1, Myotonic dystrophy type 1, Steinert disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=273]
processing orphanet number: 1931 ...  .. annotations: 11
processing orphanet number: 60039 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43430
processing orphanet number: 85337 ...  .. annotations: 3
processing orphanet number: 85338 ...  .. annotations: 3
processing orphanet number: 85335 ...  .. annotations: 19
adding alternatives:[X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - Seizures, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1568, Fried syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85335]
processing orphanet number: 85336 ...  .. annotations: 4
processing orphanet number: 85334 ...  .. annotations: 6
processing orphanet number: 85331 ...  .. annotations: 6
processing orphanet number: 1937 ...  .. annotations: 10
adding alternatives:[Eng-Strom syndrome, Short stature - locking fingers, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1937]
processing orphanet number: 85332 ...  .. annotations: 2
adding alternatives:[X-linked intellectual disability-retinitis pigmentosa syndrome, Aldred syndrome, Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion, Retinitis pigmentosa and intellectual disability due to del(X)(p11.3), Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85332]
processing orphanet number: 60030 ...  .. annotations: 29
processing orphanet number: 85330 ...  .. annotations: 3
processing orphanet number: 250923 ...  .. annotations: 8
adding alternatives:[Isolated aniridia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=250923]
processing orphanet number: 52416 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1933 ...  .. annotations: 20
adding alternatives:[Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria, Booth-Haworth-Dilling syndrome, Mitochondrial encephalomyopathy - aminoacidopathy, mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1933, Mitochondrial DNA depletion syndrome, encephalomyopathic form, mtDNA depletion syndrome, encephalomyopathic form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=254803]
processing orphanet number: 52417 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 99969 ...  .. annotations: 4
processing orphanet number: 99967 ...  .. annotations: 4
adding alternatives:[Liposarcoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69078, Myxoid/round cell liposarcoma, MRCLS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99967]
processing orphanet number: 99965 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 99966 ...  .. annotations: 16
adding alternatives:[Familial rhabdoid tumor, RTPS, Rhabdoid tumor predisposition syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231108, Rhabdoid tumor, Malignant rhabdoid tumor, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69077, Atypical teratoid rhabdoid tumor, ATRT, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99966]
processing orphanet number: 280 ...  .. annotations: 79
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=280, Pitt-Rogers-Danks syndrome, Intellectual disability - dysmorphism - intrauterine growth retardation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98788]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 281 ...  .. annotations: 25
adding alternatives:[Monosomy 5p, Cri du chat syndrome, Deletion 5p, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=281]
processing orphanet number: 284 ...  .. annotations: 45
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 285 ...  .. annotations: 60
adding alternatives:[Ehlers-Danlos syndrome, hypermobility type, BJHS, Benign joint hypermobility syndrome, EDS III, Ehlers-Danlos syndrome type 3, Ehlers-Danlos syndrome, hypermobile type, HT-EDS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=285]
  ... no hpo-term mapping for orphanet annotation: 46760
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 286 ...  .. annotations: 103
adding alternatives:[Ehlers-Danlos syndrome, vascular type, EDS IV, EDS type 4, Ehlers-Danlos syndrome type 4, Ehlers-Danlos syndrome type IV, Sack-Barabas syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=286]
  ... no hpo-term mapping for orphanet annotation: 20340
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 35750
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 35390
processing orphanet number: 287 ...  .. annotations: 74
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 289 ...  .. annotations: 50
adding alternatives:[Ellis Van Creveld syndrome, Chondroectodermal dysplasia, Mesodermic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=289]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1940 ...  .. annotations: 13
processing orphanet number: 85329 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 85324 ...  .. annotations: 4
adding alternatives:[X-linked intellectual disability, Shrimpton type, MRXS9, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85324]
processing orphanet number: 87503 ...  .. annotations: 13
adding alternatives:[Mal de Meleda, Keratosis palmoplantaris transgrediens of Siemens, Meleda disease, Transgrediens palmoplantar keratoderma of Siemens, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=87503]
processing orphanet number: 85325 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 85322 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1949 ...  .. annotations: 5
processing orphanet number: 85320 ...  .. annotations: 4
processing orphanet number: 1948 ...  .. annotations: 8
adding alternatives:[Epilepsy - microcephaly - skeletal dysplasia, Battaglia-Neri syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1948]
processing orphanet number: 85321 ...  .. annotations: 30
adding alternatives:[Deafness - intellectual disability, Martin-Probst type, Martin-Probst syndrome, X-linked deafness - intellectual disability syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85321]
processing orphanet number: 1947 ...  .. annotations: 7
adding alternatives:[Progressive epilepsy - intellectual disability, Finnish type, CLN8 disease, Northern epilepsy variant, NCL, Northern epilepsy variant, Neuronal ceroid lipofuscinosis, Northern epilepsy variant, Northern epilepsy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1947]
processing orphanet number: 52429 ...  .. annotations: 18
processing orphanet number: 1946 ...  .. annotations: 10
adding alternatives:[Amelo-cerebro-hypohidrotic syndrome, Epilepsy - dementia - amelogenesis imperfecta, Kohlschutter-Tonz syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1946]
processing orphanet number: 60040 ...  .. annotations: 36
adding alternatives:[Megalencephaly-capillary malformation-polymicrogyria syndrome, MCAP, MCM, MCMTC, Macrocephaly - cutis marmorata telangiectatica congenita, Macrocephaly-capillary malformation syndrome, Megalencephaly - cutis marmorata telangiectatica congenita, Megalencephaly-capillary malformation syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=60040]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 95159 ...  .. annotations: 4
adding alternatives:[Hepatoerythropoietic porphyria, HEP, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95159, Porphyria cutanea tarda, PCT, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101330]
processing orphanet number: 290 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 55260
processing orphanet number: 97332 ...  .. annotations: 7
processing orphanet number: 291 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 55340
processing orphanet number: 33271 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 293 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 55180
processing orphanet number: 294 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 55220
processing orphanet number: 295 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 55180
processing orphanet number: 296 ...  .. annotations: 21
adding alternatives:[Enchondromatosis, Dyschondroplasia, Ollier disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=296]
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 97330 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 2801 ...  .. annotations: 18
adding alternatives:[Juvenile Paget disease, Familial osteoectasia, Hereditary hyperphosphatasia, Hyperostosid corticalis deformans juvenilis, JPG, Juvenile Paget's disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2801]
processing orphanet number: 1954 ...  .. annotations: 9
adding alternatives:[Congenital lethal erythroderma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1954]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1952 ...  .. annotations: 10
adding alternatives:[Pacman dysplasia, Epiphyseal stippling syndrome - osteoclastic hyperplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1952]
processing orphanet number: 1951 ...  .. annotations: 10
adding alternatives:[Epilepsy telangiectasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1951]
processing orphanet number: 280794 ...  .. annotations: 3
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 2808 ...  .. annotations: 4
adding alternatives:[Laryngeal abductor paralysis, Familial vocal cord dysfunction, Gerhardt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2808]
processing orphanet number: 2807 ...  .. annotations: 10
adding alternatives:[Choroid plexus carcinoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251899, Papilloma of choroid plexus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2807]
processing orphanet number: 2805 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2804 ...  .. annotations: 29
adding alternatives:[W syndrome, Pallister-W syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2804]
processing orphanet number: 1956 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 1955 ...  .. annotations: 16
adding alternatives:[Spinocerebellar ataxia type 34, Erythrokeratodermia with ataxia, SCA34, Spinocerebellar ataxia and erythrokeratodermia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1955]
processing orphanet number: 2802 ...  .. annotations: 12
adding alternatives:[X-linked sideroblastic anemia and ataxia, X-linked sideroblastic anemia with ataxia, XLSA-A, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2802]
processing orphanet number: 2812 ...  .. annotations: 14
adding alternatives:[Parana hard-skin syndrome, Hard-skin syndrome, Parana type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2812]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1964 ...  .. annotations: 14
adding alternatives:[Extrasystoles - short stature - hyperpigmentation - microcephaly, Char-Douglas-Dungan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1964]
processing orphanet number: 1962 ...  .. annotations: 6
adding alternatives:[Exostoses - anetodermia - brachydactyly type E, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1962]
processing orphanet number: 280785 ...  .. annotations: 7
processing orphanet number: 220295 ...  .. annotations: 19
processing orphanet number: 2819 ...  .. annotations: 10
processing orphanet number: 2818 ...  .. annotations: 5
adding alternatives:[Spastic paraplegia - glaucoma - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2818]
processing orphanet number: 1969 ...  .. annotations: 21
processing orphanet number: 1968 ...  .. annotations: 32
adding alternatives:[Flat face - microstomia - ear anomaly, Blepharophimosis - telecanthus - microstomia, Simosa-Penchaszadeh-Bustos syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1968]
processing orphanet number: 2815 ...  .. annotations: 14
adding alternatives:[Spastic paraparesis - deafness, Wells-Jankovic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2815]
processing orphanet number: 42642 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 93311 ...  .. annotations: 12
adding alternatives:[Multiple epiphyseal dysplasia type 5, EDM5, MED5, Polyepiphyseal dysplasia type 5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93311]
processing orphanet number: 91132 ...  .. annotations: 3
adding alternatives:[Ichthyosis-hypotrichosis syndrome, Hypotrichosis-congenital ichthyosis syndrome, IFAH syndrome, IHS, Ichthyosis-follicular atrophoderma-hypotrichosis syndrome, Ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91132]
processing orphanet number: 91133 ...  .. annotations: 13
processing orphanet number: 300878 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 93317 ...  .. annotations: 22
adding alternatives:[Spondylometaphyseal dysplasia, Sedaghatian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93317]
processing orphanet number: 91138 ...  .. annotations: 26
adding alternatives:[Cryoglobulinemic vasculitis, Essential cryoglobulinemia, Essential mixed cryoglobulinemia, MC, Mixed cryoglobulinemia, Primary cryoglobulinemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91138]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 90289 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 20160
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 93316 ...  .. annotations: 11
adding alternatives:[Spondylometaphyseal dysplasia, Schmidt type, Spondylometaphyseal dysplasia with severe genu valgum, Spondylometaphyseal dysplasia, Algerian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93316]
processing orphanet number: 93315 ...  .. annotations: 18
adding alternatives:[Spondylometaphyseal dysplasia, 'corner fracture' type, Spondylometaphyseal dysplasia, Sutcliffe type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93315]
processing orphanet number: 93314 ...  .. annotations: 22
adding alternatives:[Spondylometaphyseal dysplasia, Kozlowski type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93314]
processing orphanet number: 79492 ...  .. annotations: 2
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 91131 ...  .. annotations: 15
adding alternatives:[DK1-CDG, CDG syndrome type Im, CDG-Im, CDG1M, Carbohydrate deficient glycoprotein syndrome type Im, Congenital disorder of glycosylation type 1m, Congenital disorder of glycosylation type Im, Dolichol kinase deficiency, Hypotonia and ichthyosis due to dolichol phosphate deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91131]
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 166100 ...  .. annotations: 13
adding alternatives:[Stickler syndrome type 3, Stickler syndrome, non-ocular type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166100]
processing orphanet number: 2823 ...  .. annotations: 16
adding alternatives:[Paraplegia - brachydactyly - cone-shaped epiphysis, Fitzsimmons-Guilbert syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2823]
processing orphanet number: 2822 ...  .. annotations: 13
adding alternatives:[Autosomal recessive spastic paraplegia type 11, Nakamura-Osame syndrome, SPG11, Spastic paraplegia - intellectual disability - thin corpus callosum, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2822]
processing orphanet number: 1974 ...  .. annotations: 34
adding alternatives:[Autosomal recessive facio-digito-genital syndrome, Aarskog-like syndrome, Facio-digito-genital syndrome, Kuwait type, Teebi-Naguib-Alawadi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1974]
processing orphanet number: 2821 ...  .. annotations: 10
adding alternatives:[Spastic paraplegia - neuropathy - poikiloderma, Antinolo-Nieto-Borrego syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2821]
processing orphanet number: 1973 ...  .. annotations: 16
adding alternatives:[Faciocardiorenal syndrome, Eastman-Bixler syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1973]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2820 ...  .. annotations: 13
adding alternatives:[Spastic paraplegia - nephritis - deafness, Fitzsimmons-Walson-Mellor syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2820]
processing orphanet number: 1972 ...  .. annotations: 18
adding alternatives:[Lethal faciocardiomelic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1972]
processing orphanet number: 1970 ...  .. annotations: 28
adding alternatives:[Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1970]
  ... no hpo-term mapping for orphanet annotation: 24400
processing orphanet number: 93308 ...  .. annotations: 13
adding alternatives:[Multiple epiphyseal dysplasia type 1, EDM1, MED1, Polyepiphyseal dysplasia type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93308]
processing orphanet number: 93307 ...  .. annotations: 12
adding alternatives:[Multiple epiphyseal dysplasia type 4, Autosomal recessive multiple epiphyseal dysplasia, EDM4, MED4, Polyepiphyseal dysplasia type 4, rMED, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93307]
processing orphanet number: 1979 ...  .. annotations: 29
adding alternatives:[Lipodystrophy due to peptidic growth factors deficiency, Combined insulin, insulin-like growth factor 1 (IGF1) and epidermal growth factor (EGF) deficiency, Hoepffner-Dreyer-Reimers syndrome, Werner-like syndrome due to combined growth factor deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1979]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2826 ...  .. annotations: 7
adding alternatives:[Spastic paraplegia - precocious puberty, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2826]
processing orphanet number: 71519 ...  .. annotations: 3
processing orphanet number: 2825 ...  .. annotations: 10
adding alternatives:[PARC syndrome, Poikiloderma - alopecia - retrognathism - cleft palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2825]
processing orphanet number: 2824 ...  .. annotations: 19
adding alternatives:[Paraplegia - intellectual disability - hyperkeratosis, Fitzsimmons-McLachlan-Gilbert syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2824]
processing orphanet number: 93302 ...  .. annotations: 10
adding alternatives:[Brachyolmia, Maroteaux type, Brachyolmia type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93302]
processing orphanet number: 93301 ...  .. annotations: 9
adding alternatives:[Brachyolmia type 1, Hobaek type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93301]
processing orphanet number: 268249 ...  .. annotations: 27
processing orphanet number: 93304 ...  .. annotations: 8
adding alternatives:[Autosomal dominant brachyolmia, Brachyolmia type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93304]
processing orphanet number: 93303 ...  .. annotations: 12
adding alternatives:[Brachyolmia type 1, Toledo type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93303]
processing orphanet number: 79481 ...  .. annotations: 1
processing orphanet number: 79480 ...  .. annotations: 6
processing orphanet number: 2834 ...  .. annotations: 36
adding alternatives:[Wrinkly skin syndrome, WSS, Wrinkled skin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2834, Autosomal recessive cutis laxa type 2A, ARCL2A, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=357058]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1986 ...  .. annotations: 4
adding alternatives:[Gollop-Wolfgang complex, Bifid femur - monodactylous ectrodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1986]
processing orphanet number: 2833 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 2832 ...  .. annotations: 6
adding alternatives:[Short tarsus - absence of lower eyelashes, Lopes-Gorlin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2832]
processing orphanet number: 2831 ...  .. annotations: 16
adding alternatives:[Rhizomelic dysplasia, Patterson-Lowry type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2831]
processing orphanet number: 1980 ...  .. annotations: 12
processing orphanet number: 1509 ...  .. annotations: 6
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1509]
processing orphanet number: 1508 ...  .. annotations: 10
adding alternatives:[Coxoauricular syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1508]
processing orphanet number: 2839 ...  .. annotations: 28
adding alternatives:[Pelvis-shoulder dysplasia, Kosenow syndrome, Scapuloiliac dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2839]
processing orphanet number: 1507 ...  .. annotations: 81
adding alternatives:[Autosomal recessive Robinow syndrome, COVESDEM syndrome, Costovertebral segmentation defect - mesomelia, RRS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1507, Robinow syndrome, Acral dysostosis with facial and genital abnormalities, Fetal face syndrome, Mesomelic dwarfism-small genitalia syndrome, Robinow dwarfism, Robinow-Silverman-Smith syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97360]
processing orphanet number: 2838 ...  .. annotations: 5
processing orphanet number: 1506 ...  .. annotations: 9
processing orphanet number: 2837 ...  .. annotations: 16
adding alternatives:[Pellagra-like skin rash - neurological manifestations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2837]
processing orphanet number: 1505 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2836 ...  .. annotations: 40
adding alternatives:[PEHO syndrome, Progressive encephalopathy - optic atrophy, Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2836, PEHO-like syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99807]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1988 ...  .. annotations: 36
adding alternatives:[Femoral-facial syndrome, FFS, FHUFS, Femoral hypoplasia - unusual facies syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1988]
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 2835 ...  .. annotations: 14
adding alternatives:[Pectus excavatum - macrocephaly - dysplastic nails, Zori-Stalker-Williams syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2835]
processing orphanet number: 67047 ...  .. annotations: 8
adding alternatives:[3-methylglutaconic aciduria type 3, Autosomal recessive optic atrophy plus syndrome, Autosomal recessive optic atrophy type 3, Costeff optic atrophy syndrome, Costeff syndrome, Infantile optic atrophy with chorea and spastic paraplegia, MGA3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=67047]
processing orphanet number: 67048 ...  .. annotations: 11
adding alternatives:[3-methylglutaconic aciduria type 4, MGA4, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=67048]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 67046 ...  .. annotations: 6
adding alternatives:[3-methylglutaconic aciduria type 1, 3-methylglutaconyl-CoA hydratase deficiency, 3MG-CoA hydratase deficiency, MGA type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=67046]
processing orphanet number: 35099 ...  .. annotations: 12
processing orphanet number: 35098 ...  .. annotations: 11
processing orphanet number: 35093 ...  .. annotations: 5
processing orphanet number: 1514 ...  .. annotations: 14
NO OMIMENTRY FOR OMIM-ID 312860 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 1513 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 1997 ...  .. annotations: 14
adding alternatives:[Blepharo-cheilo-odontic syndrome, BCD syndrome, Blepharocheilodontic syndrome, Clefting - ectropion - conical teeth, Ectropion inferior - cleft lip and or palate, Elsching syndrome, Lagophthalmia - cleft lip and palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1997]
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 1512 ...  .. annotations: 22
NO OMIMENTRY FOR OMIM-ID 218090 creating NEW one
processing orphanet number: 1995 ...  .. annotations: 4
processing orphanet number: 2842 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 2841 ...  .. annotations: 6
adding alternatives:[Familial benign chronic pemphigus, Benign chronic familial pemphigus of Hailey-Hailey, Hailey-Hailey disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2841]
processing orphanet number: 1993 ...  .. annotations: 16
adding alternatives:[Pai syndrome, Median cleft of the upper lip - corpus callosum lipoma - cutaneous polyps, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1993]
  ... no hpo-term mapping for orphanet annotation: 23740
processing orphanet number: 2840 ...  .. annotations: 11
adding alternatives:[Pelvic dysplasia - arthrogryposis of lower limbs, Ray-Peterson-Scott syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2840]
processing orphanet number: 281201 ...  .. annotations: 4
adding alternatives:[Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome, KLICK syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=281201]
processing orphanet number: 1991 ...  .. annotations: 3
processing orphanet number: 1519 ...  .. annotations: 40
adding alternatives:[Hypertelorism, Teebi type, Brachycephalofrontonasal dysplasia, Craniofrontonasal dysplasia, Teebi type, Teebi hypertelorism syndrome, Teebi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1519]
processing orphanet number: 93329 ...  .. annotations: 25
adding alternatives:[Omodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2733, Autosomal recessive omodysplasia, Micromelic dysplasia - dislocation of radius, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93329]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2849 ...  .. annotations: 32
adding alternatives:[Perlman syndrome, Nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2849]
processing orphanet number: 1517 ...  .. annotations: 38
adding alternatives:[Hypertrichotic osteochondrodysplasia, Cantu type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1517]
processing orphanet number: 1516 ...  .. annotations: 30
adding alternatives:[Craniofacial dyssynostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1516]
processing orphanet number: 2847 ...  .. annotations: 9
processing orphanet number: 67041 ...  .. annotations: 3
adding alternatives:[Hyaluronidase deficiency, MPS9, MPSIX, Mucopolysaccharidosis type 9, Mucopolysaccharidosis type IX, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=67041]
processing orphanet number: 1515 ...  .. annotations: 31
processing orphanet number: 2846 ...  .. annotations: 5
processing orphanet number: 93328 ...  .. annotations: 18
adding alternatives:[Omodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2733, Autosomal dominant omodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93328]
processing orphanet number: 300865 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 95501 ...  .. annotations: 3
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 166119 ...  .. annotations: 6
adding alternatives:[Isolated osteopoikilosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166119, Buschke-Ollendorff syndrome, Disseminated dermatofibrosis with osteopoikilosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1306]
processing orphanet number: 90291 ...  .. annotations: 59
adding alternatives:[CREST syndrome, Calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90290, Systemic sclerosis, Systemic scleroderma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90291]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 90290 ...  .. annotations: 16
adding alternatives:[CREST syndrome, Calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90290, Systemic sclerosis, Systemic scleroderma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90291]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 2856 ...  .. annotations: 4
adding alternatives:[Persistent Müllerian duct syndrome, PMDS, Persistent Müllerian derivatives, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2856]
processing orphanet number: 1525 ...  .. annotations: 16
adding alternatives:[Cranio-osteoarthropathy, Currarino disease, Currarino idiopathic osteoarthropathy, Reginato-Schiapachasse syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1525, Pachydermoperiostosis, PDP, Touraine-Solente-Gole syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2796]
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 2855 ...  .. annotations: 20
processing orphanet number: 1524 ...  .. annotations: 39
NO OMIMENTRY FOR OMIM-ID 602558 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2854 ...  .. annotations: 25
adding alternatives:[Fuhrmann syndrome, Fibular hypoplasia or aplasia - femoral bowing - oligodactyly, Fuhrmann-Rieger-de Sousa syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2854]
processing orphanet number: 1522 ...  .. annotations: 14
processing orphanet number: 1520 ...  .. annotations: 42
adding alternatives:[Craniofrontonasal dysplasia, CFND, CFNS, Craniofrontonasal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1520]
processing orphanet number: 2850 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1529 ...  .. annotations: 17
adding alternatives:[Craniofacial-deafness-hand syndrome, CDHS, Sommer-Young-Wee-Frye syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1529]
processing orphanet number: 1528 ...  .. annotations: 16
adding alternatives:[Craniotelencephalic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1528]
processing orphanet number: 1527 ...  .. annotations: 4
adding alternatives:[Craniosynostosis, Philadelphia type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1527, Syndactyly type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93402]
processing orphanet number: 93357 ...  .. annotations: 26
adding alternatives:[SPONASTRIME dysplasia, Spondyloepimetaphyseal dysplasia, Sponastrime type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93357]
processing orphanet number: 93356 ...  .. annotations: 12
adding alternatives:[Metaphyseal anadysplasia, Maroteaux-Verloes-Stanescu syndrome, Regressive metaphyseal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1040, Spondyloepimetaphyseal dysplasia, Missouri type, SEMD type 2, SEMD, Missouri type, Spondyloepimetaphyseal dysplasia type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93356]
processing orphanet number: 93359 ...  .. annotations: 33
adding alternatives:[Spondyloepimetaphyseal dysplasia with joint laxity, SEMD-JL, SEMDJL1, Spondyloepimetaphyseal dysplasia with joint laxity type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93359]
processing orphanet number: 93352 ...  .. annotations: 23
adding alternatives:[Spondyloepimetaphyseal dysplasia, Shohat type, SEMD, Shohat type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93352]
processing orphanet number: 93351 ...  .. annotations: 17
adding alternatives:[Spondyloepimetaphyseal dysplasia, Irapa type, SEMD type Irapa, SEMD, Irapa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93351]
processing orphanet number: 1535 ...  .. annotations: 10
processing orphanet number: 2866 ...  .. annotations: 7
processing orphanet number: 2865 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 1533 ...  .. annotations: 29
adding alternatives:[Craniosynostosis - fibular aplasia, Lowry syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1533]
processing orphanet number: 1532 ...  .. annotations: 20
adding alternatives:[Gómez-López-Hernández syndrome, Cerebellotrigeminal - dermal dysplasia, Craniosynostosis - alopecia - brain defect, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1532]
processing orphanet number: 2863 ...  .. annotations: 25
NO OMIMENTRY FOR OMIM-ID 185120 creating NEW one
processing orphanet number: 1530 ...  .. annotations: 3
processing orphanet number: 2869 ...  .. annotations: 34
adding alternatives:[Peutz-Jeghers syndrome, Hamartomatous intestinal polyposis, PJS, Polyps and spots syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2869]
  ... no hpo-term mapping for orphanet annotation: 50010
processing orphanet number: 1538 ...  .. annotations: 12
adding alternatives:[Craniosynostosis - Dandy-Walker malformation - hydrocephalus, Braddock-Jones-Superneau syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1538]
processing orphanet number: 2868 ...  .. annotations: 13
adding alternatives:[Short stature - valvular heart disease - characteristic facies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2868]
processing orphanet number: 93346 ...  .. annotations: 25
adding alternatives:[Spondyloepimetaphyseal dysplasia congenita, Strudwick type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93346]
processing orphanet number: 36397 ...  .. annotations: 27
adding alternatives:[Adiposis dolorosa, Adiposalgia, Adipose tissue rheumatism, Dercum's disease, Lipomatosis dolorosa, Neurolipomatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=36397]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 40540
processing orphanet number: 2881 ...  .. annotations: 5
adding alternatives:[Cutaneous photosensitivity - lethal colitis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2881]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1547 ...  .. annotations: 9
adding alternatives:[Cryptomicrotia - brachydactyly - excess fingertip arch, Cryptomicrotia-brachydactyly syndrome, Tonoki-Ohura-Niikawa syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1547]
processing orphanet number: 2878 ...  .. annotations: 21
adding alternatives:[Phocomelia - ectrodactyly - deafness - sinus arrhythmia, Stoll-Lévy-Francfort syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2878]
processing orphanet number: 1545 ...  .. annotations: 24
NO OMIMENTRY FOR OMIM-ID 601378 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2876 ...  .. annotations: 27
NO OMIMENTRY FOR OMIM-ID 261575 creating NEW one
processing orphanet number: 2875 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 4260
processing orphanet number: 2872 ...  .. annotations: 28
adding alternatives:[Cardiocranial syndrome, Pfeiffer type, Craniosynostosis - congenital heart disease - intellectual disability, Pfeiffer-Singer-Zschiesche syndrome, Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2872]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1541 ...  .. annotations: 10
NO OMIMENTRY FOR OMIM-ID 604757 creating NEW one
processing orphanet number: 35069 ...  .. annotations: 8
processing orphanet number: 1540 ...  .. annotations: 21
adding alternatives:[Jackson-Weiss syndrome, Craniosynostosis - midfacial hypoplasia - foot abnormalities, JWS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1540]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 2871 ...  .. annotations: 18
adding alternatives:[Pfeiffer-Palm-Teller syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2871]
processing orphanet number: 47045 ...  .. annotations: 17
adding alternatives:[Familial cold urticaria, FCAS, FCAS1, FCU, Familial cold autoinflammatory syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=47045]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 48377 ...  .. annotations: 7
processing orphanet number: 48372 ...  .. annotations: 2
processing orphanet number: 1548 ...  .. annotations: 17
processing orphanet number: 2879 ...  .. annotations: 29
adding alternatives:[Phocomelia, Schinzel type, Al Awadi-Raas-Rothschild syndrome, Aplasia/hypoplasia of limbs and pelvis, Congenital absence of ulna and fibula, Severe limb deficit, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2879]
processing orphanet number: 2892 ...  .. annotations: 17
adding alternatives:[Pilodental dysplasia - refractive errors, Euhidrotic ectodermal dysplasia, Kopysc-Barczyk-Krol syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2892]
processing orphanet number: 2891 ...  .. annotations: 11
adding alternatives:[Pili torti - developmental delay - neurological abnormalities, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2891]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2890 ...  .. annotations: 4
processing orphanet number: 2405 ...  .. annotations: 4
adding alternatives:[Thickened earlobes - conductive deafness, Escher-Hirt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2405]
processing orphanet number: 2889 ...  .. annotations: 11
adding alternatives:[Pili torti, Twisted hair, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2889]
processing orphanet number: 2888 ...  .. annotations: 23
adding alternatives:[Pierre Robin syndrome - faciodigital anomaly, Chitayat-Meunier-Hodgkinson syndrome, Pierre Robin sequence - faciodigital anomaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2888]
processing orphanet number: 1556 ...  .. annotations: 31
adding alternatives:[Cutis marmorata telangiectatica congenita, CMTC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1556]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 1555 ...  .. annotations: 42
adding alternatives:[Cutis gyrata - acanthosis nigricans - craniosynostosis, Beare-Stevenson cutis gyrata syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1555]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 2886 ...  .. annotations: 8
adding alternatives:[TARP syndrome, Pierre Robin sequence - congenital heart defect - talipes, Pierre Robin syndrome - congenital heart defect - talipes, Talipes equinovarus - atrial septal defect - Robin sequence - Persistence of the left superior vena cava, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2886]
processing orphanet number: 2885 ...  .. annotations: 15
adding alternatives:[Piebald trait - neurologic defects, Telfer-Sugar-Jaeger syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2885]
processing orphanet number: 1553 ...  .. annotations: 22
adding alternatives:[Curry-Jones syndrome, Corpus callosum agenesis - polysyndactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1553]
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2400 ...  .. annotations: 7
adding alternatives:[Peripheral motor neuropathy - dysautonomia, Lisker-Garcia-Ramos syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2400]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 2884 ...  .. annotations: 20
adding alternatives:[Piebaldism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2884]
processing orphanet number: 1552 ...  .. annotations: 12
adding alternatives:[Currarino triad, Currarino syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1552]
processing orphanet number: 1551 ...  .. annotations: 14
adding alternatives:[Familial benign copper deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1551]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 250984 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 2409 ...  .. annotations: 39
adding alternatives:[Lowry-MacLean syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2409]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2408 ...  .. annotations: 5
processing orphanet number: 2407 ...  .. annotations: 15
adding alternatives:[LOC syndrome, LOGIC syndrome, Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome, Laryngo-onycho-cutaneous syndrome, Shabbir syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2407]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 250989 ...  .. annotations: 48
adding alternatives:[1q21.1 microdeletion syndrome, Del(1)(q21), Monosomy 1q21.1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=250989]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2406 ...  .. annotations: 14
processing orphanet number: 1572 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 93360 ...  .. annotations: 37
adding alternatives:[Spondyloepimetaphyseal dysplasia with multiple dislocations, SEMD-MD, SEMDJL2, Spondyloepimetaphyseal dysplasia with joint laxicity, Hall type, Spondyloepimetaphyseal dysplasia with joint laxity type 2, Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type, Spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93360]
processing orphanet number: 1571 ...  .. annotations: 25
adding alternatives:[Knobloch syndrome, Knobloch-Layer syndrome, Retinal detachment - occipital encephalocele, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1571]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1570 ...  .. annotations: 8
processing orphanet number: 1568 ...  .. annotations: 8
adding alternatives:[X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - Seizures, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1568, Fried syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85335]
processing orphanet number: 2414 ...  .. annotations: 19
adding alternatives:[Congenital pulmonary lymphangiectasia, Pulmonary lymphangiomatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2414]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2898 ...  .. annotations: 5
adding alternatives:[X-linked intellectual disability - plagiocephaly, Hyde Forster-McCarthy-Berry syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2898]
processing orphanet number: 2897 ...  .. annotations: 14
adding alternatives:[Pityriasis rubra pilaris, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2897]
processing orphanet number: 1566 ...  .. annotations: 3
adding alternatives:[Dandy-Walker malformation - postaxial polydactyly, DWM with postaxial polydactyly, Pierquin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1566]
processing orphanet number: 2412 ...  .. annotations: 20
adding alternatives:[Dislocation of the hip - dysmorphism, Collins-Pope syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2412]
processing orphanet number: 250994 ...  .. annotations: 25
adding alternatives:[1q21.1 microduplication syndrome, Dup(1)(q21.1), Trisomy 1q21.1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=250994]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2896 ...  .. annotations: 24
adding alternatives:[Pitt-Hopkins syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2896]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1564 ...  .. annotations: 7
processing orphanet number: 1563 ...  .. annotations: 18
adding alternatives:[Dahlberg-Borer-Newcomer syndrome, Dahlberg syndrome, Lymphedema - hypoparathyroidism syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1563]
processing orphanet number: 2410 ...  .. annotations: 5
adding alternatives:[Hypergonadotropic hypogonadism - cataract syndrome, Lubinsky syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2410]
processing orphanet number: 2894 ...  .. annotations: 21
processing orphanet number: 1562 ...  .. annotations: 3
adding alternatives:[Dacryocystitis - osteopoikilosis, Gunal-Seber-Basaran syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1562]
processing orphanet number: 46724 ...  .. annotations: 3
adding alternatives:[Cerebral arteriovenous malformation, Cerebral arteriovenous fistula, Cerebral arteriovenous shunt, Intracranial arteriovenous malformation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46724]
processing orphanet number: 238446 ...  .. annotations: 18
adding alternatives:[15q11q13 microduplication syndrome, 15q11-q13 duplication syndrome, 15q11-q13 microduplication syndrome, 15q11q13 duplication syndrome, Dup(15)(q11q13), Trisomy 15q11-q13, Trisomy 15q11q13, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238446]
processing orphanet number: 2430 ...  .. annotations: 2
adding alternatives:[Congenital macroglossia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2430]
processing orphanet number: 1581 ...  .. annotations: 15
processing orphanet number: 1580 ...  .. annotations: 31
NO OMIMENTRY FOR OMIM-ID 601362 creating NEW one
processing orphanet number: 2427 ...  .. annotations: 15
processing orphanet number: 1577 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1574 ...  .. annotations: 8
adding alternatives:[Retinal degeneration - nanophthalmos - glaucoma, Mackay-Shek-Carr syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1574]
processing orphanet number: 1573 ...  .. annotations: 16
adding alternatives:[Hypotrichosis with juvenile macular degeneration, HJMD, Hypotrichosis with juvenile macular dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1573]
processing orphanet number: 93947 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 93946 ...  .. annotations: 11
processing orphanet number: 2429 ...  .. annotations: 26
adding alternatives:[Macrocephaly - spastic paraplegia - dysmorphism, Fryns macrocephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2429]
processing orphanet number: 178045 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 261211 ...  .. annotations: 39
adding alternatives:[16p11.2p12.2 microdeletion syndrome, 16p11.2-p12.2 microdeletion syndrome, Del(16)(p11.2p12.2), Monosomy 16p11.2-p12.2, Monosomy 16p11.2p12.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261211]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1110 ...  .. annotations: 24
adding alternatives:[Aortic arch anomaly - peculiar facies - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1110]
processing orphanet number: 2440 ...  .. annotations: 9
processing orphanet number: 1590 ...  .. annotations: 22
NO OMIMENTRY FOR OMIM-ID 602553 creating NEW one
processing orphanet number: 52183 ...  .. annotations: 14
adding alternatives:[Autosomal recessive primary microcephaly, MCPH, Microcephalia vera, Microcephaly vera, True microcephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2512, Premature chromosome condensation with microcephaly and intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52183]
  ... no hpo-term mapping for orphanet annotation: 52000
processing orphanet number: 2438 ...  .. annotations: 24
adding alternatives:[Hand-foot-genital syndrome, HFGS, Hand-foot-uterus syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2438]
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 1106 ...  .. annotations: 37
adding alternatives:[Microphthalmia with limb anomalies, Anophthalmia-syndactyly syndrome, OAS, Ophthalmoacromelic syndrome, Waardenburg anophthalmia syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1106]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2437 ...  .. annotations: 28
adding alternatives:[Czeizel-Losonci syndrome, Split hand - urinary anomalies - spina bifida, Split hand with obstructive uropathy, spina bifida and diaphragmatic defects, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2437]
processing orphanet number: 1104 ...  .. annotations: 17
adding alternatives:[Anophthalmia plus syndrome, Fryns microphthalmia syndrome, Microphthalmia with facial clefting, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1104]
processing orphanet number: 2435 ...  .. annotations: 9
adding alternatives:[Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual disability, Westerhof-Beemer-Cormane syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2435]
processing orphanet number: 1587 ...  .. annotations: 31
adding alternatives:[Monosomy 13q14, Del(13)(q14), Deletion 13q14, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1587]
processing orphanet number: 2432 ...  .. annotations: 13
adding alternatives:[Macrosomia - microphthalmia - cleft palate, Teebi-Al Saleh-Hassoon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2432]
  ... no hpo-term mapping for orphanet annotation: 53000
processing orphanet number: 1101 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 2431 ...  .. annotations: 7
processing orphanet number: 33408 ...  .. annotations: 5
processing orphanet number: 33409 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 2439 ...  .. annotations: 15
adding alternatives:[Patterson-Stevenson-Fontaine syndrome, Patterson-Stevenson syndrome, Split foot deformity - mandibulofacial dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2439]
processing orphanet number: 238468 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1120 ...  .. annotations: 26
adding alternatives:[Lung agenesis - heart defect - thumb anomalies, Mardini--Nyhan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1120]
processing orphanet number: 2451 ...  .. annotations: 3
adding alternatives:[Mucocutaneous venous malformations, Cutaneous and mucosal venous malformation, VMCM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2451]
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 261204 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1118 ...  .. annotations: 5
adding alternatives:[Fibular aplasia - ectrodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1118]
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 1117 ...  .. annotations: 11
adding alternatives:[Aplasia cutis - myopia, Gershoni-Baruch-Leibo syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1117]
processing orphanet number: 1116 ...  .. annotations: 13
adding alternatives:[Aplasia cutis congenita - intestinal lymphangiectasia, Autosomal recessive aplasia cutis, Bronspiegel-Zelnick syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1116]
processing orphanet number: 1115 ...  .. annotations: 6
adding alternatives:[Recessive aplasia cutis congenita of limbs, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1115]
processing orphanet number: 1598 ...  .. annotations: 31
adding alternatives:[Monosomy 18p, 18p- syndrome, De Grouchy syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1598]
processing orphanet number: 2445 ...  .. annotations: 6
adding alternatives:[Conotruncal heart malformations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2445, Truncus arteriosus, Common aortico-pulmonary trunk, Common arterial trunk, TAC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3384, Double outlet right ventricle, DORV, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3426]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1114 ...  .. annotations: 9
adding alternatives:[Aplasia cutis congenita, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1114]
processing orphanet number: 2444 ...  .. annotations: 6
processing orphanet number: 1597 ...  .. annotations: 33
processing orphanet number: 1113 ...  .. annotations: 15
adding alternatives:[Aphalangy - syndactyly - microcephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1113]
processing orphanet number: 1112 ...  .. annotations: 18
adding alternatives:[Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis, Johnson-Munson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1112]
processing orphanet number: 2442 ...  .. annotations: 8
processing orphanet number: 2463 ...  .. annotations: 30
adding alternatives:[Marfanoid habitus - intellectual disability, autosomal recessive, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2463]
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 1132 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1131 ...  .. annotations: 25
adding alternatives:[X-linked mandibulofacial dysostosis, Mandibulofacial dysostosis, Toriello type, X-linked branchial arch syndrome, X-linked mandibulofacial dysostosis with limb anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1131]
processing orphanet number: 2462 ...  .. annotations: 55
adding alternatives:[Shprintzen-Goldberg syndrome, Marfanoid craniosynostosis syndrome, SGS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2462]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2461 ...  .. annotations: 40
adding alternatives:[Marden-Walker syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2461]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1130 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2460 ...  .. annotations: 33
adding alternatives:[Van den Ende-Gupta syndrome, Marden-Walker-like syndrome, VDEGS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2460]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 3307 ...  .. annotations: 18
NO OMIMENTRY FOR OMIM-ID 614290 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 1129 ...  .. annotations: 24
processing orphanet number: 3305 ...  .. annotations: 18
processing orphanet number: 169105 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 2457 ...  .. annotations: 40
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3304 ...  .. annotations: 18
adding alternatives:[Fallot complex - intellectual disability - growth delay, Bindewald-Ulmer-Müller syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3304]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3303 ...  .. annotations: 13
adding alternatives:[Tetralogy of Fallot, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3303]
processing orphanet number: 2456 ...  .. annotations: 3
adding alternatives:[Familial supernumerary nipples, Isolated polythelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2456]
processing orphanet number: 2454 ...  .. annotations: 8
adding alternatives:[Familial intestinal malrotation - facial anomalies, Stalker-Chitayat syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2454]
processing orphanet number: 3301 ...  .. annotations: 30
adding alternatives:[Tetraamelia - multiple malformations, Zimmer phocomelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3301]
processing orphanet number: 1123 ...  .. annotations: 21
processing orphanet number: 1122 ...  .. annotations: 2
adding alternatives:[Ulnar hypoplasia - split foot, Ulnar hypoplasia - lobster-claw deformity of feet, Van den Berghe-Dequecker syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1122]
processing orphanet number: 700 ...  .. annotations: 2
processing orphanet number: 701 ...  .. annotations: 6
processing orphanet number: 702 ...  .. annotations: 36
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 703 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 23330
processing orphanet number: 704 ...  .. annotations: 10
adding alternatives:[Pemphigus vulgaris, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=704]
processing orphanet number: 705 ...  .. annotations: 14
adding alternatives:[Pendred syndrome, Goiter - deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=705]
processing orphanet number: 706 ...  .. annotations: 20
NO OMIMENTRY FOR OMIM-ID 607411 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 55260
processing orphanet number: 708 ...  .. annotations: 12
adding alternatives:[Peters anomaly, Peters congenital glaucoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=708]
processing orphanet number: 709 ...  .. annotations: 65
adding alternatives:[Peters plus syndrome, Krause-Kivlin syndrome, Krause-van Schooneveld-Kivlin syndrome, Peters anomaly with short limb dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=709]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 90000 ...  .. annotations: 9
processing orphanet number: 261265 ...  .. annotations: 21
adding alternatives:[17q12 microdeletion syndrome, Del(17)(q12), Monosomy 17q12, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261265]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1143 ...  .. annotations: 22
adding alternatives:[Neurogenic arthrogryposis multiplex congenita, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1143]
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 3320 ...  .. annotations: 34
adding alternatives:[Thrombocytopenia - absent radius, TAR syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3320]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2473 ...  .. annotations: 28
adding alternatives:[McKusick-Kaufman syndrome, Hydrometrocolpos - postaxial polydactyly, Kaufman-Mckusick syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2473]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2471 ...  .. annotations: 28
adding alternatives:[McDonough syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2471]
processing orphanet number: 2470 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 166024 ...  .. annotations: 18
adding alternatives:[Multiple epiphyseal dysplasia, Al-Gazali type, Multiple epiphyseal dysplasia - macrocephaly - distinctive facies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166024]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 3318 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 35720
processing orphanet number: 3317 ...  .. annotations: 10
processing orphanet number: 3316 ...  .. annotations: 12
processing orphanet number: 2467 ...  .. annotations: 34
processing orphanet number: 3314 ...  .. annotations: 6
adding alternatives:[Thiemann disease, familial form, Aseptic necrosis of phalangeal epiphyses, Osteochondritis of phalangeal epiphyses, Osteochondrosis of phalangeal epiphyses, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3314]
processing orphanet number: 1135 ...  .. annotations: 12
adding alternatives:[Arrhinia - choanal atresia - microphthalmia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1135, Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism, Bosma-Henkin-Christiansen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2250]
processing orphanet number: 2466 ...  .. annotations: 12
adding alternatives:[MASA syndrome, Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2466, L1 syndrome, CRASH syndrome, Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome, L1CAM syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=275543]
processing orphanet number: 710 ...  .. annotations: 23
adding alternatives:[Pfeiffer syndrome, ACS5, Acrocephalosyndactyly type 5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=710]
processing orphanet number: 3312 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 1134 ...  .. annotations: 6
processing orphanet number: 1133 ...  .. annotations: 28
adding alternatives:[AREDYLD syndrome, Acrorenal defect - ectodermal dysplasia - diabetes, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1133]
processing orphanet number: 3311 ...  .. annotations: 9
NO OMIMENTRY FOR OMIM-ID 273490 creating NEW one
processing orphanet number: 716 ...  .. annotations: 4
adding alternatives:[Phenylketonuria, PAH deficiency, PKU, Phenylalanine hydroxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=716, Maternal phenylketonuria, Hyperphenylalaninemic embryopathy, Maternal PKU, Maternal hyperphenylalaninemia, Phenylketonuric embryopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2209]
processing orphanet number: 717 ...  .. annotations: 3
processing orphanet number: 718 ...  .. annotations: 5
adding alternatives:[Isolated Pierre Robin syndrome, Isolated Pierre Robin sequence, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=718]
processing orphanet number: 178487 ...  .. annotations: 9
processing orphanet number: 3319 ...  .. annotations: 12
adding alternatives:[Congenital amegakaryocytic thrombocytopenia, CAMT, Congenital amegakaryocytic thrombocytopenic purpura, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3319]
processing orphanet number: 261250 ...  .. annotations: 46
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 178481 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1154 ...  .. annotations: 18
adding alternatives:[Arthrogryposis with oculomotor limitation and electroretinal anomalies, Distal arthrogryposis type 5, Distal arthrogryposis type IIB, Distal arthrogryposis with ophthalmoplegia, Oculomelic amyoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1154]
processing orphanet number: 2001 ...  .. annotations: 17
adding alternatives:[Cleft lip/palate - intestinal malrotation - cardiopathy, McPherson-Clemens syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2001]
processing orphanet number: 2485 ...  .. annotations: 20
adding alternatives:[Melorheostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2485]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3332 ...  .. annotations: 14
adding alternatives:[Absent tibia - polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=988, Hypoplastic tibiae - postaxial polydactyly, Werner mesomelic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3332]
processing orphanet number: 2484 ...  .. annotations: 38
adding alternatives:[Melnick-Needles syndrome, Melnick-Needles osteodysplasty, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2484]
processing orphanet number: 3331 ...  .. annotations: 15
processing orphanet number: 2483 ...  .. annotations: 14
adding alternatives:[Melkersson-Rosenthal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2483]
  ... no hpo-term mapping for orphanet annotation: 23490
processing orphanet number: 166016 ...  .. annotations: 11
adding alternatives:[Multiple epiphyseal dysplasia, Lowry type, Multiple epiphyseal dysplasia with Robin phenotype, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166016]
processing orphanet number: 2482 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 1150 ...  .. annotations: 27
adding alternatives:[Arthrogryposis multiplex congenita - whistling face, Illum syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1150]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 2481 ...  .. annotations: 27
adding alternatives:[Neurocutaneous melanocytosis, NCM, Neurocutaneous melanosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2481]
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 3329 ...  .. annotations: 17
processing orphanet number: 3328 ...  .. annotations: 16
adding alternatives:[Absent tibia - polydactyly - arachnoid cyst, Holmes-Collins syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3328]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 1149 ...  .. annotations: 11
adding alternatives:[Arthrogryposis-like syndrome, Kuskokwim disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1149]
processing orphanet number: 3327 ...  .. annotations: 14
adding alternatives:[Thyrocerebrorenal syndrome, Cutler-Bass-Romshe syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3327]
processing orphanet number: 2479 ...  .. annotations: 40
adding alternatives:[Megalocornea-intellectual disability syndrome, MMR syndrome, Neuhäuser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2479]
processing orphanet number: 3326 ...  .. annotations: 19
adding alternatives:[Thymic-renal-anal-lung dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3326]
processing orphanet number: 1147 ...  .. annotations: 21
adding alternatives:[Sheldon-Hall syndrome, Distal Arthrogryposis type 2B, Freeman-Sheldon syndrome variant, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1147]
processing orphanet number: 1146 ...  .. annotations: 10
processing orphanet number: 2477 ...  .. annotations: 17
processing orphanet number: 720 ...  .. annotations: 2
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1145 ...  .. annotations: 30
adding alternatives:[X-linked distal arthrogryposis multiplex congenita, SMAX2, SMAX2-related spinal muscular atrophy, Spinal muscular atrophy with arthrogryposis, X-linked infantile spinal muscular atrophy, X-linked spinal muscular atrophy type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1145]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2476 ...  .. annotations: 9
processing orphanet number: 3323 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 55520
processing orphanet number: 721 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 38640
processing orphanet number: 1144 ...  .. annotations: 6
adding alternatives:[Arthrogryposis-like hand anomaly - sensorineural deafness, Distal arthrogryposis type 6, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1144]
processing orphanet number: 2475 ...  .. annotations: 20
adding alternatives:[White forelock with malformations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2475]
processing orphanet number: 3322 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 722 ...  .. annotations: 11
adding alternatives:[Hypoplasminogenemia, Plasminogen deficiency type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=722, Ligneous conjunctivitis, Conjunctivitis lignosa, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97231]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 724 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 726 ...  .. annotations: 10
adding alternatives:[Alpers-Huttenlocher syndrome, Alpers progressive sclerosing poliodystrophy, Alpers syndrome, Progressive neuronal degeneration of childhood with liver disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=726]
processing orphanet number: 727 ...  .. annotations: 39
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 178478 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 728 ...  .. annotations: 63
  ... no hpo-term mapping for orphanet annotation: 8840
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 178475 ...  .. annotations: 14
processing orphanet number: 729 ...  .. annotations: 25
adding alternatives:[Polycythemia vera, Acquired primary erythocytosis, Erythremia, Osler-Vaquez disease, PV, Polycythemia rubra vera, Vaquez disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=729]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 3800
processing orphanet number: 95712 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 95713 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90024 ...  .. annotations: 24
adding alternatives:[Deafness with labyrinthine aplasia, microtia, and microdontia, LAMM syndrome, Microdontia - type I microtia - deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90024]
processing orphanet number: 95714 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 90023 ...  .. annotations: 10
adding alternatives:[Primary immunodeficiency syndrome due to p14 deficiency, Primary immunodeficiency syndrome with short stature, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90023]
processing orphanet number: 95715 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 261243 ...  .. annotations: 18
processing orphanet number: 50809 ...  .. annotations: 5
adding alternatives:[Talo-patello-scaphoid osteolysis, Singh-Williams-McAlister syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50809]
processing orphanet number: 95711 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2496 ...  .. annotations: 42
adding alternatives:[Mesomelia-synostoses syndrome, 8q13 microdeletion syndrome, Del(8)q(13), Mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type, Mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type, Monosomy 8q13, Verloes-David syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2496]
processing orphanet number: 1164 ...  .. annotations: 13
adding alternatives:[Allergic bronchopulmonary aspergillosis, ABPA, Allergic aspergillosis, Hinson-Pepys disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1164]
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 3342 ...  .. annotations: 46
adding alternatives:[Arterial tortuosity syndrome, ATS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3342]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 35720
processing orphanet number: 2494 ...  .. annotations: 9
adding alternatives:[Menetrier disease, Giant hypertrophic gastritis, Hypoproteinemic hypertrophic gastropathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2494]
processing orphanet number: 2010 ...  .. annotations: 9
adding alternatives:[Cleft palate - stapes fixation - oligodontia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2010]
processing orphanet number: 3341 ...  .. annotations: 29
adding alternatives:[Torticollis - keloids - cryptorchidism - renal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3341]
processing orphanet number: 2492 ...  .. annotations: 10
processing orphanet number: 79230 ...  .. annotations: 11
processing orphanet number: 1160 ...  .. annotations: 7
adding alternatives:[Chylous ascites, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1160]
processing orphanet number: 2491 ...  .. annotations: 15
adding alternatives:[Müllerian duct anomalies - limb anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2491]
processing orphanet number: 79234 ...  .. annotations: 9
adding alternatives:[Crigler-Najjar syndrome, Bilirubin uridinediphosphate glucuronosyltransferase deficiency, Bilirubin-UGT deficiency, Hereditary unconjugated hyperbilirubinemia, UGT deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=205, Crigler-Najjar syndrome type 1, Bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1, Bilirubin-UGT deficiency type 1, Hereditary unconjugated hyperbilirubinemia type 1, UGT deficiency type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79234]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2008 ...  .. annotations: 38
adding alternatives:[Acro-cardio-facial syndrome, ACFS, CCGE syndrome, Cleft palate - cardiac defect - genital anomalies - ectrodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2008]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3339 ...  .. annotations: 28
adding alternatives:[Toriello-Lacassie-Droste syndrome, Aplasia cutis congenita - epibulbar dermoids, Oculoectodermal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3339]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2007 ...  .. annotations: 7
adding alternatives:[Alar cartilages hypoplasia-coloboma-telecanthus syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2007]
processing orphanet number: 3338 ...  .. annotations: 55
adding alternatives:[Toriello-Carey syndrome, Corpus callosum agenesis - blepharophimosis - Robin sequence, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3338]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1159 ...  .. annotations: 11
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1159]
processing orphanet number: 2006 ...  .. annotations: 1
processing orphanet number: 79235 ...  .. annotations: 2
adding alternatives:[Crigler-Najjar syndrome, Bilirubin uridinediphosphate glucuronosyltransferase deficiency, Bilirubin-UGT deficiency, Hereditary unconjugated hyperbilirubinemia, UGT deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=205, Crigler-Najjar syndrome type 2, Arias syndrome, Bilirubin uridinediphosphate glucuronosyltransferase deficiency type 2, Bilirubin-UGT deficiency type 2, Hereditary unconjugated hyperbilirubinemia type 2, UGT deficiency type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79235]
processing orphanet number: 2005 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 730 ...  .. annotations: 20
processing orphanet number: 2489 ...  .. annotations: 12
adding alternatives:[Upper limb defect - eye and ear abnormalities, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2489]
processing orphanet number: 79238 ...  .. annotations: 13
adding alternatives:[Galactosemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352, Galactose epimerase deficiency, Epimerase deficiency galactosemia, GALE deficiency, GALE-D, Galactosemia type 3, UDP-galactose-4-epimerase deficiency, Uridine diphosphate galactose-4-epimerase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79238]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 731 ...  .. annotations: 15
adding alternatives:[Autosomal recessive polycystic kidney disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=731]
processing orphanet number: 2004 ...  .. annotations: 2
adding alternatives:[Laryngo-tracheo-esophageal cleft, LC, LTEC, Laryngo-tracheo-esophageal diastema, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2004, Laryngo-tracheo-esophageal cleft type 3, LTEC III, LTEC3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93940]
processing orphanet number: 79237 ...  .. annotations: 3
adding alternatives:[Galactosemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352, Galactokinase deficiency, GALK deficiency, GALK-D, Galactokinase deficiency galactosemia, Galactosemia type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79237]
processing orphanet number: 732 ...  .. annotations: 40
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 2003 ...  .. annotations: 13
processing orphanet number: 2487 ...  .. annotations: 15
processing orphanet number: 733 ...  .. annotations: 12
adding alternatives:[Familial adenomatous polyposis, Colorectal adenomatous polyposis, FAP, Familial polyposis coli, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=733, APC-related attenuated familial adenomatous polyposis, APC-related AFAP, APC-related attenuated FAP, APC-related attenuated familial polyposis coli, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=247806, Attenuated familial adenomatous polyposis, AFAP, Attenuated FAP, Attenuated familial polyposis coli, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=220460, Gardner syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79665, Turcot syndrome with polyposis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99818]
  ... no hpo-term mapping for orphanet annotation: 45510
processing orphanet number: 1155 ...  .. annotations: 17
adding alternatives:[Arthrogryposis due to muscular dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1155]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 2486 ...  .. annotations: 2
processing orphanet number: 79239 ...  .. annotations: 22
adding alternatives:[Galactosemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352, Classic galactosemia, GALT deficiency, Galactose-1-phosphate uridyltransferase deficiency, Galactosemia type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79239]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 735 ...  .. annotations: 7
processing orphanet number: 178029 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 737 ...  .. annotations: 4
adding alternatives:[Porokeratosis plantaris palmaris et disseminata, Palmar, plantar and disseminated porokeratosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=737]
processing orphanet number: 738 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 50811 ...  .. annotations: 12
adding alternatives:[Lipodystrophy - intellectual disability - deafness, Rajab-Spranger syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50811]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 739 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 50810 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 50812 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 50815 ...  .. annotations: 17
adding alternatives:[Branchiogenic deafness syndrome, Mégarbané-Loiselet syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50815]
processing orphanet number: 50814 ...  .. annotations: 34
adding alternatives:[Craniolenticulosutural dysplasia, Boyadjiev-Jabs syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50814]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 50817 ...  .. annotations: 13
processing orphanet number: 42775 ...  .. annotations: 28
adding alternatives:[PHACE syndrome, Pascual-Castroviejo syndrome type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=42775]
processing orphanet number: 3354 ...  .. annotations: 43
adding alternatives:[Tricho-oculo-dermo-vertebral syndrome, Alves-dos Santos-Castelo syndrome, Ectodermal dysplasia - cataracts - kyphoscoliosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3354]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2022 ...  .. annotations: 16
adding alternatives:[Endomyocardial fibroelastosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2022]
processing orphanet number: 3353 ...  .. annotations: 20
processing orphanet number: 1174 ...  .. annotations: 12
adding alternatives:[Cerebellar ataxia - ectodermal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1174]
processing orphanet number: 2021 ...  .. annotations: 30
processing orphanet number: 261236 ...  .. annotations: 36
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3352 ...  .. annotations: 20
adding alternatives:[Tricho-dento-osseous syndrome, TDO syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3352]
processing orphanet number: 2020 ...  .. annotations: 8
processing orphanet number: 1173 ...  .. annotations: 18
processing orphanet number: 3351 ...  .. annotations: 12
adding alternatives:[Trichodental syndrome, Kersey syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3351]
processing orphanet number: 3350 ...  .. annotations: 5
adding alternatives:[Tremor - nystagmus - duodenal ulcer, Neuhauser-Daly-Magnelli syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3350]
processing orphanet number: 1171 ...  .. annotations: 9
adding alternatives:[Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss, CAPOS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1171]
processing orphanet number: 1170 ...  .. annotations: 15
adding alternatives:[Autosomal recessive cerebelloparenchymal disorder type 3, SCAR2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1170]
processing orphanet number: 2019 ...  .. annotations: 8
NO OMIMENTRY FOR OMIM-ID 228200 creating NEW one
processing orphanet number: 2017 ...  .. annotations: 2
processing orphanet number: 740 ...  .. annotations: 43
adding alternatives:[Hutchinson-Gilford progeria syndrome, HGPS, Progeria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=740]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 2016 ...  .. annotations: 11
adding alternatives:[Cleft palate-lateral synechia syndrome, CPLS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2016]
processing orphanet number: 3347 ...  .. annotations: 3
adding alternatives:[Mounier-Kühn syndrome, Congenital tracheobronchomegaly, Idiopathic tracheobronchomegaly, Tracheobronchomegaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3347]
processing orphanet number: 3346 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 55680
processing orphanet number: 1168 ...  .. annotations: 4
adding alternatives:[Ataxia - oculomotor apraxia type 1, AOA1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1168]
processing orphanet number: 742 ...  .. annotations: 40
adding alternatives:[Prolidase deficiency, Hyperimidodipeptiduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=742]
processing orphanet number: 2499 ...  .. annotations: 10
adding alternatives:[Metachondromatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2499]
processing orphanet number: 2015 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 2014 ...  .. annotations: 2
adding alternatives:[Cleft palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2014]
processing orphanet number: 2498 ...  .. annotations: 2
adding alternatives:[Syndactyly type 8, Fusion of metacarpals 4 and 5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2498]
processing orphanet number: 743 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 1167 ...  .. annotations: 5
processing orphanet number: 744 ...  .. annotations: 95
adding alternatives:[Proteus syndrome, Partial gigantism - nevi - hemihypertrophy - macrocephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=744]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 50070
processing orphanet number: 1166 ...  .. annotations: 28
adding alternatives:[Congenital unilateral hypoplasia of depressor anguli oris, Isolated asymmetric crying facies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1166]
processing orphanet number: 2013 ...  .. annotations: 22
adding alternatives:[Cleft palate - large ears - small head, Say-Barber-Hobbs syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2013]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 2497 ...  .. annotations: 4
adding alternatives:[Upper limb mesomelic dysplasia, Fryns-Hofkens-Fabry syndrome, Ulna hypoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2497]
processing orphanet number: 3344 ...  .. annotations: 18
adding alternatives:[Weismann-Netter syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3344]
processing orphanet number: 745 ...  .. annotations: 11
processing orphanet number: 1187 ...  .. annotations: 15
adding alternatives:[Lethal ataxia with deafness and optic atrophy, Arts syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1187]
processing orphanet number: 3365 ...  .. annotations: 15
processing orphanet number: 1186 ...  .. annotations: 7
adding alternatives:[Infantile onset spinocerebellar ataxia, IOSCA, Ohaha syndrome, Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1186]
processing orphanet number: 2033 ...  .. annotations: 12
processing orphanet number: 1185 ...  .. annotations: 28
adding alternatives:[Spinocerebellar ataxia - dysmorphism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1185]
processing orphanet number: 3363 ...  .. annotations: 22
adding alternatives:[Trichomegaly - retina pigmentary degeneration - dwarfism, Long eyelashes - intellectual disability, Oliver-McFarlane syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3363]
processing orphanet number: 1184 ...  .. annotations: 16
processing orphanet number: 2031 ...  .. annotations: 29
adding alternatives:[Hepatic fibrosis - renal cysts - intellectual disability, Thompson-Baraitser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2031]
processing orphanet number: 96147 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3361 ...  .. annotations: 10
adding alternatives:[Trichodysplasia - xeroderma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3361]
processing orphanet number: 1182 ...  .. annotations: 9
adding alternatives:[Spastic ataxia with congenital miosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1182]
processing orphanet number: 3360 ...  .. annotations: 10
processing orphanet number: 1180 ...  .. annotations: 3
adding alternatives:[Ataxia - hypogonadism - choroidal dystrophy, Boucher-Neuhäuser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1180]
processing orphanet number: 251014 ...  .. annotations: 64
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2029 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 45510
processing orphanet number: 750 ...  .. annotations: 24
adding alternatives:[Pseudoachondroplasia, Pseudoachondroplastic dysplasia, Pseudoachondroplastic spondyloepiphyseal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=750]
processing orphanet number: 2028 ...  .. annotations: 16
adding alternatives:[Juvenile hyaline fibromatosis, Murray-Puretic-Drescher syndrome, Puretic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2028]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 752 ...  .. annotations: 9
adding alternatives:[46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency, 17-beta-hydroxysteroid dehydrogenase 3 deficiency, 17-ketoreductase deficiency, 17-ketosteroidreductase deficiency, Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=752]
processing orphanet number: 2027 ...  .. annotations: 4
adding alternatives:[Gingival fibromatosis - progressive deafness, Jones syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2027]
processing orphanet number: 753 ...  .. annotations: 11
adding alternatives:[46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency, 46,XY DSD due to 5-alpha-reductase 2 deficiency, Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency, Pseudovaginal perineoscrotal hypospadias, Steroid 5-alpha-reductase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=753]
processing orphanet number: 1179 ...  .. annotations: 4
adding alternatives:[Benign paroxysmal tonic upgaze of childhood with ataxia, Ouvrier-Billson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1179]
processing orphanet number: 2026 ...  .. annotations: 14
adding alternatives:[Gingival fibromatosis-hypertrichosis syndrome, CGHT, Congenital generalized hypertrichosis terminalis, Hirsutism-congenital gingival hyperplasia syndrome, Hypertrichose avec ou sans hyperplasie gingivale, Hypertrichosis with or without gingival hyperplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2026]
  ... no hpo-term mapping for orphanet annotation: 24400
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 3357 ...  .. annotations: 6
processing orphanet number: 754 ...  .. annotations: 8
processing orphanet number: 1178 ...  .. annotations: 9
adding alternatives:[Ataxia - tapetoretinal degeneration, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1178]
processing orphanet number: 2025 ...  .. annotations: 14
adding alternatives:[Gingival fibromatosis - facial dysmorphism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2025]
processing orphanet number: 2024 ...  .. annotations: 2
processing orphanet number: 3355 ...  .. annotations: 13
adding alternatives:[Trichoodontoonychial dysplasia, Trichoodontoonychial dysplasia with bone deficiency in frontoparietal region, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3355]
processing orphanet number: 757 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 758 ...  .. annotations: 47
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 35390
processing orphanet number: 231401 ...  .. annotations: 12
adding alternatives:[Alpha-thalassemia-myelodysplastic syndrome, ATMDS, Acquired HbH disease, Acquired hemoglobin H disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231401]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 251019 ...  .. annotations: 40
adding alternatives:[2q32q33 microdeletion syndrome, 2q32-q33 microdeletion syndrome, Del(2)(q32), Del(2)(q32q33), Monosomy 2q32, Monosomy 2q32-q33, Monosomy 2q32q33, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251019]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 261295 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 3376 ...  .. annotations: 35
processing orphanet number: 1198 ...  .. annotations: 9
adding alternatives:[Colonic atresia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1198]
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2045 ...  .. annotations: 8
processing orphanet number: 3375 ...  .. annotations: 18
processing orphanet number: 2044 ...  .. annotations: 43
adding alternatives:[Floating-Harbor syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2044]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 3374 ...  .. annotations: 19
processing orphanet number: 1195 ...  .. annotations: 8
adding alternatives:[Congenital atransferrinemia, Congenital hypotransferrinemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1195]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 2042 ...  .. annotations: 10
processing orphanet number: 1194 ...  .. annotations: 28
adding alternatives:[TMEM70-related mitochondrial encephalo-cardio-myopathy, Mitochondrial encephalo-cardio-myopathy due to F1Fo ATPase deficiency, Mitochondrial encephalo-cardio-myopathy due to isolated ATP synthase deficiency, Mitochondrial encephalo-cardio-myopathy due to isolated mitochondrial respiratory chain complex V deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1194]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2040 ...  .. annotations: 2
processing orphanet number: 1193 ...  .. annotations: 15
adding alternatives:[Atkin-Flaitz syndrome, X-linked intellectual disability, Atkin type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1193]
processing orphanet number: 98791 ...  .. annotations: 33
adding alternatives:[Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16, ATR syndrome linked to chromosome 16, ATR syndrome, deletion type, ATR-16 syndrome, Alpha thalassemia-intellectual disability syndrome, deletion type, Alpha thalassemia-retardation syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98791]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1192 ...  .. annotations: 22
adding alternatives:[Atherosclerosis - deafness - diabetes - epilepsy - nephropathy, Feigenbaum-Bergeron-Richardson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1192]
processing orphanet number: 49827 ...  .. annotations: 14
adding alternatives:[Thiamine-responsive megaloblastic anemia syndrome, Rogers syndrome, TRMA, Thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=49827]
processing orphanet number: 761 ...  .. annotations: 36
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 763 ...  .. annotations: 42
adding alternatives:[Pycnodysostosis, Pyknodysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=763]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 3369 ...  .. annotations: 18
adding alternatives:[Trigonocephaly - short stature - developmental delay, Say-Meyer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3369]
processing orphanet number: 3368 ...  .. annotations: 11
adding alternatives:[Trigonocephaly - bifid nose - acral anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3368]
processing orphanet number: 764 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 35664 ...  .. annotations: 4
adding alternatives:[De Barsy syndrome, Cutis laxa - corneal clouding - intellectual disability, Progeroid syndrome, De Barsy type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2962, ALDH18A1-related De Barsy syndrome, Delta-1-pyrroline 5-carboxylate synthetase deficiency, Neurocutaneous syndrome, Bicknell type, P5CS deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35664]
processing orphanet number: 765 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 2036 ...  .. annotations: 23
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2036]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 1188 ...  .. annotations: 18
adding alternatives:[Ataxia-deafness-intellectual disability syndrome, Reardon-Baraitser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1188]
processing orphanet number: 3366 ...  .. annotations: 7
processing orphanet number: 33001 ...  .. annotations: 26
adding alternatives:[Lymphedema - distichiasis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33001]
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 767 ...  .. annotations: 60
  ... no hpo-term mapping for orphanet annotation: 35750
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 35720
processing orphanet number: 768 ...  .. annotations: 7
processing orphanet number: 89843 ...  .. annotations: 9
adding alternatives:[Dystrophic epidermolysis bullosa pruriginosa, DEB, pruriginosa, DEB-Pr, Pruriginous dystrophic epidermolysis bullosa, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89843]
processing orphanet number: 769 ...  .. annotations: 27
adding alternatives:[Rabson-Mendenhall syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=769]
processing orphanet number: 89842 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 46240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 89841 ...  .. annotations: 3
processing orphanet number: 89840 ...  .. annotations: 17
adding alternatives:[Localized junctional epidermolysis bullosa, non-Herlitz type, JEB-nH loc, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251393, Junctional epidermolysis bullosa, non-Herlitz type, JEN-nH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89840, Generalized junctional epidermolysis bullosa, non-Herlitz type, GABEB, Generalized atrophic benign epidermolysis bullosa, JEB-nH gen, Junctional epidermolysis bullosa generalisata mitis, Junctional epidermolysis bullosa, Disentis type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79402, Junctional epidermolysis bullosa inversa, EBJ-I, Inverse JEB, JEB-I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79405]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3387 ...  .. annotations: 9
adding alternatives:[Isolated anterior cervical hypertrichosis, Hairy throat syndrome, Tsukahara-Kajii syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3387]
processing orphanet number: 96167 ...  .. annotations: 44
adding alternatives:[Recombinant 8 syndrome, Duplication 8q/deletion 8p, Rec(8) syndrome, Rec8 syndrome, Recombinant chromosome 8 syndrome, San Luis Valley syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=96167]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2053 ...  .. annotations: 33
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 96169 ...  .. annotations: 56
adding alternatives:[Koolen-De Vries syndrome, KdVS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=96169]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2052 ...  .. annotations: 52
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2052]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 3383 ...  .. annotations: 13
adding alternatives:[Humerus trochlea aplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3383]
processing orphanet number: 2050 ...  .. annotations: 26
processing orphanet number: 3380 ...  .. annotations: 66
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 770 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 771 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 772 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 773 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 774 ...  .. annotations: 34
processing orphanet number: 2048 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 775 ...  .. annotations: 2
  ... no hpo-term mapping for orphanet annotation: 55520
processing orphanet number: 3378 ...  .. annotations: 58
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 776 ...  .. annotations: 33
processing orphanet number: 2047 ...  .. annotations: 32
adding alternatives:[Flynn-Aird syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2047]
processing orphanet number: 3377 ...  .. annotations: 8
adding alternatives:[Trismus - pseudocamptodactyly, Distal arthrogryposis type 7, Dutch-Kentucky syndrome, Hecht syndrome, Hecht-Beals syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3377]
processing orphanet number: 777 ...  .. annotations: 2
processing orphanet number: 778 ...  .. annotations: 38
adding alternatives:[Rett syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=778, Atypical Rett syndrome, Atypical RTT, Rett syndrome variant, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3095]
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 254509 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 779 ...  .. annotations: 26
adding alternatives:[Reynolds syndrome, Primary biliary cirrhosis and systemic scleroderma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=779]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 254504 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 261290 ...  .. annotations: 50
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3390 ...  .. annotations: 14
adding alternatives:[Proximal tubulopathy - diabetes mellitus - cerebellar ataxia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3390]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 49804 ...  .. annotations: 6
processing orphanet number: 261272 ...  .. annotations: 15
adding alternatives:[17q12 microduplication syndrome, Dup(17)(q12), Trisomy 17q12, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261272]
processing orphanet number: 164736 ...  .. annotations: 8
processing orphanet number: 261279 ...  .. annotations: 45
adding alternatives:[17q23.1q23.2 microdeletion syndrome, 17q23.1-q23.2 microdeletion syndrome, Del(17)(q23.1q23.2), Monosomy 17q23.1-q23.2, Monosomy 17q23.1q23.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261279]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2067 ...  .. annotations: 56
adding alternatives:[GAPO syndrome, Growth delay - alopecia - pseudoanodontia - optic atrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2067]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23740
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3398 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 63259 ...  .. annotations: 18
processing orphanet number: 2065 ...  .. annotations: 27
adding alternatives:[Galloway-Mowat syndrome, Galloway syndrome, Microcephaly - hiatus hernia - nephrotic syndrome, Nephrosis - neuronal dysmigration syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2065]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 75234 ...  .. annotations: 15
adding alternatives:[Lysosomal acid lipase deficiency, LAL deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=275761, Cholesteryl ester storage disease, Cholesterol ester storage disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75234, Wolman disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75233]
processing orphanet number: 2064 ...  .. annotations: 8
adding alternatives:[Posterior fusion of lumbosacral vertebrae - blepharoptosis, Faulk-Epstein-Jones syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2064]
processing orphanet number: 75233 ...  .. annotations: 18
adding alternatives:[Lysosomal acid lipase deficiency, LAL deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=275761, Cholesteryl ester storage disease, Cholesterol ester storage disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75234, Wolman disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75233]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2063 ...  .. annotations: 32
adding alternatives:[Splenogonadal fusion - limb defects - micrognathia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2063]
processing orphanet number: 2062 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 2060 ...  .. annotations: 12
processing orphanet number: 782 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 783 ...  .. annotations: 41
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2059 ...  .. annotations: 51
adding alternatives:[Fryns syndrome, Diaphragmatic hernia - abnormal face - distal limb anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2059]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 302 ...  .. annotations: 13
processing orphanet number: 2058 ...  .. annotations: 19
processing orphanet number: 303 ...  .. annotations: 52
  ... no hpo-term mapping for orphanet annotation: 20160
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 304 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2057 ...  .. annotations: 14
adding alternatives:[Blepharophimosis - ptosis - esotropia - syndactyly - short stature, Frydman-Cohen-Karmon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2057]
processing orphanet number: 305 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 306 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 63261 ...  .. annotations: 18
adding alternatives:[Retinal vasculopathy and cerebral leukodystrophy, RVCL, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=247691, Cerebroretinal vasculopathy, CRV, Grand-Kaine-Fulling syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3421, HERNS syndrome, Hereditary endotheliopathy - retinopathy - nephropathy - stroke, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=63261, Hereditary vascular retinopathy, HVR, Hereditary vascular retinopathy - Raynaud phenomenon - migraine, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=71291]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 47612 ...  .. annotations: 35
adding alternatives:[Felty syndrome, Splenomegaly-neutropenia-rheumatoid arthritis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=47612]
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 158008 ...  .. annotations: 2
processing orphanet number: 2078 ...  .. annotations: 26
adding alternatives:[Geroderma osteodysplastica, Walt Disney dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2078]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2077 ...  .. annotations: 31
adding alternatives:[German syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2077]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2076 ...  .. annotations: 2
processing orphanet number: 2075 ...  .. annotations: 27
adding alternatives:[Genito-palato-cardiac syndrome, Gardner-Silengo-Wachtel syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2075]
processing orphanet number: 2074 ...  .. annotations: 15
processing orphanet number: 2073 ...  .. annotations: 10
processing orphanet number: 790 ...  .. annotations: 2
adding alternatives:[Retinoblastoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=790]
processing orphanet number: 2072 ...  .. annotations: 13
adding alternatives:[Gaucher disease, Acid beta-glucosidase deficiency, Glucocerebrosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355, Gaucher disease - ophthalmoplegia - cardiovascular calcification, Cardiovascular Gaucher disease, Gaucher disease type 3C, Gaucher-like disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2072]
processing orphanet number: 791 ...  .. annotations: 29
processing orphanet number: 792 ...  .. annotations: 7
adding alternatives:[X-linked retinoschisis, X-linked juvenile retinoschisis, XLRS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=792]
processing orphanet number: 793 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 794 ...  .. annotations: 38
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=794]
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 796 ...  .. annotations: 21
adding alternatives:[Sandhoff disease, GM2 gangliosidosis 0 variant, Hexosaminidases A and B deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=796, Sandhoff disease, infantile form, Hexosaminidases A and B deficiency, infantile form, Infantile GM2 gangliosidosis 0 variant, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=309155, Sandhoff disease, adult form, Adult GM2 gangliosidosis 0 variant, Hexosaminidases A and B deficiency, adult form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=309169, Sandhoff disease, juvenile form, Hexosaminidases A and B deficiency, juvenile form, Juvenile GM2 gangliosidosis 0 variant, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=309162]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 312 ...  .. annotations: 10
processing orphanet number: 313 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 2069 ...  .. annotations: 14
adding alternatives:[Gastrocutaneous syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2069]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 798 ...  .. annotations: 71
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=798]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 314 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 799 ...  .. annotations: 8
adding alternatives:[Schizencephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=799]
processing orphanet number: 251056 ...  .. annotations: 30
NO OMIMENTRY FOR OMIM-ID 612863 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 315 ...  .. annotations: 3
processing orphanet number: 316 ...  .. annotations: 3
processing orphanet number: 317 ...  .. annotations: 31
adding alternatives:[Transgrediens et progrediens palmoplantar keratoderma, Greither disease, Keratosis extremitatum hereditaria progrediens, Keratosis palmoplantaris transgrediens et progrediens, Progressive diffuse PPK, Progressive diffuse palmoplantar keratoderma, Transgrediens et progrediens PPK, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=495, Erythrokeratodermia variabilis, EKV, Erythrokeratodermia variabilis, Mendes da Costa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=317]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 158014 ...  .. annotations: 7
processing orphanet number: 63260 ...  .. annotations: 7
processing orphanet number: 2081 ...  .. annotations: 7
processing orphanet number: 63275 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 251071 ...  .. annotations: 37
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2085 ...  .. annotations: 2
adding alternatives:[Glaucoma - sleep apnea, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2085]
processing orphanet number: 2084 ...  .. annotations: 4
adding alternatives:[Glaucoma - ectopia - microspherophakia - stiff joints - short stature, GEMSS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2084, Weill-Marchesani syndrome, Spherophakia - brachymorphia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3449]
processing orphanet number: 2083 ...  .. annotations: 30
adding alternatives:[Prominent glabella - microcephaly - hypogenitalism, Mac Dermot-Winter syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2083]
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 321 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 46000
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 33445 ...  .. annotations: 20
adding alternatives:[Neuroectodermal melanolysosomal disease, Elejalde disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33445]
processing orphanet number: 323 ...  .. annotations: 30
processing orphanet number: 324 ...  .. annotations: 66
adding alternatives:[Fabry disease, Alpha-galactosidase A deficiency, Anderson-Fabry disease, Angiokeratoma corporis diffusum, Diffuse angiokeratoma, FD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 49500
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43430
processing orphanet number: 251066 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 55654 ...  .. annotations: 12
processing orphanet number: 158003 ...  .. annotations: 4
processing orphanet number: 158000 ...  .. annotations: 9
processing orphanet number: 2092 ...  .. annotations: 70
adding alternatives:[Focal dermal hypoplasia, Goltz syndrome, Goltz-Gorlin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2092]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2091 ...  .. annotations: 6
adding alternatives:[Multinodular goiter - cystic kidney - polydactyly, Daneman-Davy-Mancer syndrome, Thyroid-renal-digital anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2091]
processing orphanet number: 158029 ...  .. annotations: 12
adding alternatives:[Sea-blue histiocytosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=158029]
processing orphanet number: 2090 ...  .. annotations: 13
adding alternatives:[GMS syndrome, Goniodysgenesis - intellectual disability - short stature, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2090]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 93930 ...  .. annotations: 14
adding alternatives:[Exstrophy-epispadias complex, BEEC, Bladder exstrophy-epispadias-cloacal extrophy complex, EEC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=322, Bladder exstrophy, Classic exstrophy of the bladder, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93930]
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2099 ...  .. annotations: 27
processing orphanet number: 2098 ...  .. annotations: 18
adding alternatives:[Acromesomelic dysplasia, Grebe type, Chondrodysplasia, Grebe type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2098]
processing orphanet number: 2097 ...  .. annotations: 25
adding alternatives:[Grant syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2097]
processing orphanet number: 2095 ...  .. annotations: 28
adding alternatives:[Gorlin-Chaudhry-Moss syndrome, Craniofacial dysostosis - genital, dental, cardiac anomalies, Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora, Dental and eye anomalies-patent ductus arteriosus-normal intelligence, GCM syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2095]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 35612 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 55180
  ... no hpo-term mapping for orphanet annotation: 55360
  ... no hpo-term mapping for orphanet annotation: 55380
processing orphanet number: 333 ...  .. annotations: 25
adding alternatives:[Farber disease, Acid ceramidase deficiency, Farber lipogranulomatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=333]
  ... no hpo-term mapping for orphanet annotation: 46240
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 251038 ...  .. annotations: 30
adding alternatives:[3q29 microduplication, Trisomy 3q29, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251038]
processing orphanet number: 337 ...  .. annotations: 21
adding alternatives:[Fibrodysplasia ossificans progressiva, FOP, Myositis ossificans progressiva, Stone man syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=337]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 46000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 338 ...  .. annotations: 3
processing orphanet number: 93929 ...  .. annotations: 22
adding alternatives:[Exstrophy-epispadias complex, BEEC, Bladder exstrophy-epispadias-cloacal extrophy complex, EEC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=322, Cloacal exstrophy, OEIS complex, Omphalocele - cloacal exstrophy - imperforate anus - spinal defect, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93929]
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 93928 ...  .. annotations: 5
processing orphanet number: 48918 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 340 ...  .. annotations: 33
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 98375 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 251046 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 341 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 342 ...  .. annotations: 39
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 343 ...  .. annotations: 28
adding alternatives:[Hyperimmunoglobulinemia D with periodic fever, HIDS, Hyper-IgD syndrome, Hyperimmunoglobinemia D with recurrent fever, Hyperimmunoglobulinemia D syndrome, Partial mevalonate kinase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=343]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 345 ...  .. annotations: 8
adding alternatives:[Dissecting cellulitis of the scalp, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=345]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 346 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 347 ...  .. annotations: 7
adding alternatives:[Frasier syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=347]
processing orphanet number: 349 ...  .. annotations: 35
adding alternatives:[Fucosidosis, Alpha-L-fucosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=349]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 158025 ...  .. annotations: 1
adding alternatives:[Hereditary progressive mucinous histiocytosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=158025]
processing orphanet number: 158022 ...  .. annotations: 5
processing orphanet number: 351 ...  .. annotations: 10
adding alternatives:[Galactosialidosis, Goldberg syndrome, Neuraminidase deficiency with beta-galactosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=351]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 352 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 354 ...  .. annotations: 50
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 49500
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 355 ...  .. annotations: 70
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 85414 ...  .. annotations: 13
NO OMIMENTRY FOR OMIM-ID 604302 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 357 ...  .. annotations: 5
processing orphanet number: 85410 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 10 ...  .. annotations: 59
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 11 ...  .. annotations: 23
processing orphanet number: 14 ...  .. annotations: 8
adding alternatives:[Abetalipoproteinemia, Bassen-Kornzweig disease, Homozygous familial hypobetalipoproteinemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=14]
processing orphanet number: 15 ...  .. annotations: 41
adding alternatives:[Achondroplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=15]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 16 ...  .. annotations: 7
adding alternatives:[Blue cone monochromatism, Atypical X-linked achromatopsia, Blue cone monochromacy, Color blindness, blue monocone monochromatic type, S cone monochromacy, S cone monochromatism, X-linked incomplete achromatopsia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=16, Progressive cone dystrophy, Cone dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1871]
processing orphanet number: 364 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 85408 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 365 ...  .. annotations: 25
adding alternatives:[Glycogen storage disease due to acid maltase deficiency, Alpha-1,4-glucosidase acid deficiency, GSD due to acid maltase deficiency, GSD type 2, Glycogen storage disease type 2, Glycogenosis due to acid maltase deficiency, Glycogenosis type 2, Pompe disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=365]
processing orphanet number: 199318 ...  .. annotations: 22
adding alternatives:[15q13.3 microdeletion syndrome, Del(15)(q13.3), Monosomy 15q13.3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=199318]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 366 ...  .. annotations: 9
adding alternatives:[Glycogen storage disease due to glycogen debranching enzyme deficiency, Amylo-1,6-glucosidase deficiency, Cori disease, Cori-Forbes disease, Forbes disease, GDE deficiency, GSD due to glycogen debranching enzyme deficiency, GSD type 3, GSDIII, Glycogen storage disease type 3, Glycogenosis due to glycogen debranching enzyme deficiency, Glycogenosis type 3, Limit dextrinosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=366]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 367 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 368 ...  .. annotations: 5
adding alternatives:[Glycogen storage disease due to muscle glycogen phosphorylase deficiency, GSD due to muscle glycogen phosphorylase deficiency, GSD type 5, Glycogen storage disease type 5, Glycogenosis due to muscle glycogen phosphorylase deficiency, Glycogenosis type 5, McArdle disease, Myophosphorylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=368]
processing orphanet number: 369 ...  .. annotations: 4
adding alternatives:[Glycogen storage disease due to liver glycogen phosphorylase deficiency, GSD due to liver glycogen phosphorylase deficiency, GSD type 6B, Glycogen storage disease type 6B, Glycogenosis due to liver glycogen phosphorylase deficiency, Glycogenosis type 6B, Hepatic glycogen phosphorylase deficiency, Hepatic phosphorylase deficiency, Hers disease, Liver glycogen phosphorylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=369]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 52503 ...  .. annotations: 24
adding alternatives:[X-linked creatine transporter deficiency, Creatine transporter deficiency, SLC6A8 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52503]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 22 ...  .. annotations: 7
adding alternatives:[4-hydroxybutyric aciduria, Succinic semialdehyde dehydrogenase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=22]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 23 ...  .. annotations: 9
adding alternatives:[Argininosuccinic aciduria, Argininosuccinase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=23]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 25 ...  .. annotations: 34
adding alternatives:[Glutaryl-CoA dehydrogenase deficiency, GA1, GCDHD, Glutaric acidemia type 1, Glutaric aciduria type 1, Glutaryl-coenzyme A dehydrogenase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=25]
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 26 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 27 ...  .. annotations: 25
adding alternatives:[Vitamin B12-unresponsive methylmalonic acidemia, Vitamin B12-unresponsive methylmalonic aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=27, Vitamin B12-unresponsive methylmalonic acidemia type mut0, Complete deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut0, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=289916, Vitamin B12-unresponsive methylmalonic acidemia type mut-, Partial deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut-, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79312]
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 28 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 29 ...  .. annotations: 17
adding alternatives:[Mevalonic aciduria, Complete mevalonate kinase deficiency, MVA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=29]
processing orphanet number: 71267 ...  .. annotations: 7
processing orphanet number: 370 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 371 ...  .. annotations: 6
adding alternatives:[Glycogen storage disease due to muscle phosphofructokinase deficiency, GSD due to muscle phosphofructokinase deficiency, GSD type 7, Glycogen storage disease type 7, Glycogenosis due to muscle phosphofructokinase deficiency, Glycogenosis type 7, Tarui disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=371]
processing orphanet number: 373 ...  .. annotations: 72
adding alternatives:[Simpson-Golabi-Behmel syndrome, DGSX, Golabi-Rosen syndrome, SDYS, SGBS, SGBS1, Simpson dysmorphia syndrome, Simpson-Golabi-Behmel syndrome type 1, X-linked dysplasia gigantism syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=373]
processing orphanet number: 374 ...  .. annotations: 44
adding alternatives:[Goldenhar syndrome, Expanded spectrum of hemifacial microsomia, Facioauriculovertebral dysplasia, OAV dysplasia, OAVS, Oculoauriculovertebral dysplasia, Oculoauriculovertebral syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=374]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 375 ...  .. annotations: 19
adding alternatives:[Anti-glomerular basement membrane disease, Anti-GBM syndrome, Goodpasture syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=375]
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 376 ...  .. annotations: 15
adding alternatives:[Gordon syndrome, Camptodactyly - cleft palate- clubfoot, Distal arthrogryposis type 3, Distal arthrogryposis type IIA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=376]
processing orphanet number: 85438 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 377 ...  .. annotations: 72
adding alternatives:[Gorlin syndrome, Basal cell nevus syndrome, Gorlin-Goltz syndrome, NBCCS, Nevoid basal cell carcinoma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=377]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 378 ...  .. annotations: 89
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 38160
processing orphanet number: 379 ...  .. annotations: 25
processing orphanet number: 251076 ...  .. annotations: 18
processing orphanet number: 85435 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 30 ...  .. annotations: 16
adding alternatives:[Hereditary orotic aciduria, Oroticaciduria, Orotidylic decarboxylase deficiency, Uridine monophosphate synthetase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=30]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 31 ...  .. annotations: 10
adding alternatives:[Oxoglutaricaciduria, Alpha-ketoglutarate dehydrogenase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=31]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 32 ...  .. annotations: 4
processing orphanet number: 33 ...  .. annotations: 4
adding alternatives:[Isovaleric acidemia, Isovaleric acid CoA dehydrogenase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33]
processing orphanet number: 35 ...  .. annotations: 12
adding alternatives:[Propionic acidemia, Ketotic hyperglycinemia, Propionic aciduria, Propionyl-CoA carboxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35]
processing orphanet number: 36 ...  .. annotations: 19
adding alternatives:[Acrocallosal syndrome, ACS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=36]
processing orphanet number: 37 ...  .. annotations: 30
adding alternatives:[Acrodermatitis enteropathica, AE, AEZ, Inherited zinc deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=37]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 38 ...  .. annotations: 7
adding alternatives:[Acrokeratoelastoidosis of Costa, AKE, PPKP3, Punctate palmoplantar hyperkeratosis type 3, Punctate palmoplantar keratoderma type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=38]
processing orphanet number: 39 ...  .. annotations: 1
processing orphanet number: 71276 ...  .. annotations: 2
processing orphanet number: 279882 ...  .. annotations: 3
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 380 ...  .. annotations: 24
adding alternatives:[Greig cephalopolysyndactyly syndrome, GCPS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=380]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 381 ...  .. annotations: 34
processing orphanet number: 384 ...  .. annotations: 8
adding alternatives:[Palmoplantar keratoderma-sclerodactyly syndrome, Huriez syndrome, Palmoplantar hyperkeratosis-sclerodactyly syndrome, Scleroatrophic syndrome, Sclerotylosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=384]
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 71270 ...  .. annotations: 21
processing orphanet number: 385 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 387 ...  .. annotations: 15
processing orphanet number: 388 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 48431 ...  .. annotations: 24
adding alternatives:[Congenital cataracts - facial dysmorphism - neuropathy, CCFDN, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=48431]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 40 ...  .. annotations: 15
adding alternatives:[Acromesomelic dysplasia, Maroteaux type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=40]
processing orphanet number: 41 ...  .. annotations: 5
adding alternatives:[Dyschromatosis symmetrica hereditaria, Acropigmentation of Dohi, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=41]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 44 ...  .. annotations: 30
processing orphanet number: 45 ...  .. annotations: 1
processing orphanet number: 47 ...  .. annotations: 33
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 2909 ...  .. annotations: 75
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2909]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 71289 ...  .. annotations: 9
adding alternatives:[Radio-ulnar synostosis - amegakaryocytic thrombocytopenia, ATRUS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=71289]
processing orphanet number: 391 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 392 ...  .. annotations: 24
adding alternatives:[Holt-Oram syndrome, Atriodigital dysplasia type 1, HOS, Heart-hand syndrome type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=392]
processing orphanet number: 393 ...  .. annotations: 5
processing orphanet number: 394 ...  .. annotations: 43
adding alternatives:[Classic homocystinuria, Cystathionine beta-synthase deficiency, Homocystinuria due to cystathionine beta-synthase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=394]
processing orphanet number: 2900 ...  .. annotations: 23
adding alternatives:[Leri pleonosteosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2900]
processing orphanet number: 396 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 86309 ...  .. annotations: 6
adding alternatives:[DPAGT1-CDG, CDG syndrome type Ij, CDG-Ij, CDG1J, Carbohydrate deficient glycoprotein syndrome type Ij, Congenital disorder of glycosylation type 1j, Congenital disorder of glycosylation type Ij, Dolichyl-phosphate N-acetylgalactosamine phosphotransferase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86309]
processing orphanet number: 397 ...  .. annotations: 57
adding alternatives:[Giant cell arteritis, Horton disease, Temporal arteritis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=397]
  ... no hpo-term mapping for orphanet annotation: 3800
  ... no hpo-term mapping for orphanet annotation: 35390
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 43430
processing orphanet number: 399 ...  .. annotations: 8
adding alternatives:[Huntington disease, Huntington chorea, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=399, Juvenile Huntington disease, JHD, Juvenile Huntington chorea, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=248111]
processing orphanet number: 86788 ...  .. annotations: 3
adding alternatives:[X-linked severe congenital neutropenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86788]
processing orphanet number: 2908 ...  .. annotations: 42
processing orphanet number: 2907 ...  .. annotations: 47
processing orphanet number: 50 ...  .. annotations: 41
adding alternatives:[Aicardi syndrome, Corpus callosum agenesis of with chorioretinal abnormality, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2905 ...  .. annotations: 23
processing orphanet number: 51 ...  .. annotations: 10
processing orphanet number: 52 ...  .. annotations: 43
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2903 ...  .. annotations: 3
adding alternatives:[Familial spontaneous pneumothorax, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2903]
processing orphanet number: 53 ...  .. annotations: 29
adding alternatives:[Albers-Schönberg osteopetrosis, Osteopetrosis autosomal dominant type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=53]
processing orphanet number: 2901 ...  .. annotations: 15
adding alternatives:[Neuralgic amyotrophy, Acute brachial plexus neuritis, Brachial plexus neuritis, Immune brachial plexus neuropathy, Mononeuritis multiplex with brachial predilection, Neuralgic shoulder amyotrophy, Serum neuritis, Winged scapula, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2901]
processing orphanet number: 54 ...  .. annotations: 14
adding alternatives:[X-linked recessive ocular albinism, OA1, Ocular albinism type 1, Ocular albinism, Nettleship-Falls type, XLOA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=54]
processing orphanet number: 55 ...  .. annotations: 17
processing orphanet number: 56 ...  .. annotations: 33
adding alternatives:[Alkaptonuria, Hereditary ochronosis, Homogentisic acid oxidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=56]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 169090 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 58 ...  .. annotations: 64
adding alternatives:[Alexander disease, AxD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=58]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43180
processing orphanet number: 59 ...  .. annotations: 24
adding alternatives:[Allan-Herndon-Dudley syndrome, AHDS, MCT8 deficiency, Monocarboxylate transporter 8 deficiency, X-linked intellectual disability - hypotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=59, Pelizaeus-Merzbacher-like disease, PMLD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=280270]
processing orphanet number: 169095 ...  .. annotations: 4
adding alternatives:[Alymphoid cystic thymic dysgenesis, Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy, Winged helix deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=169095]
processing orphanet number: 71291 ...  .. annotations: 3
adding alternatives:[Retinal vasculopathy and cerebral leukodystrophy, RVCL, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=247691, Cerebroretinal vasculopathy, CRV, Grand-Kaine-Fulling syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3421, HERNS syndrome, Hereditary endotheliopathy - retinopathy - nephropathy - stroke, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=63261, Hereditary vascular retinopathy, HVR, Hereditary vascular retinopathy - Raynaud phenomenon - migraine, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=71291]
processing orphanet number: 2911 ...  .. annotations: 33
adding alternatives:[Poland syndrome, Poland anomaly, Poland sequence, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2911]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 284804 ...  .. annotations: 10
processing orphanet number: 35107 ...  .. annotations: 38
adding alternatives:[Desmosterolosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35107]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 220393 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 40540
processing orphanet number: 182090 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2919 ...  .. annotations: 10
adding alternatives:[Orofaciodigital syndrome type 5, OFD5, Oral-facial-digital syndrome type 5, Orofaciodigital syndrome, Thurston type, Polydactyly postaxial with median cleft of upper lip, Thurston syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2919]
processing orphanet number: 60 ...  .. annotations: 6
adding alternatives:[Alpha-1-antitrypsin deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=60]
processing orphanet number: 2917 ...  .. annotations: 5
adding alternatives:[Polydactyly-myopia syndrome, Czeizel-Brooser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2917]
processing orphanet number: 61 ...  .. annotations: 43
adding alternatives:[Alpha-mannosidosis, Lysosomal alpha-D-mannosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=61]
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 2916 ...  .. annotations: 28
adding alternatives:[Postaxial polydactyly - dental and vertebral anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2916]
processing orphanet number: 63 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 64 ...  .. annotations: 55
adding alternatives:[Alström syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=64]
processing orphanet number: 65 ...  .. annotations: 16
processing orphanet number: 69 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 53000
processing orphanet number: 96129 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 96125 ...  .. annotations: 38
adding alternatives:[Distal monosomy 6p, 6p subtelomeric deletion syndrome, 6p25 microdeletion syndrome, Distal deletion 6p, Monosomy 6p25, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=96125]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2921 ...  .. annotations: 9
processing orphanet number: 2920 ...  .. annotations: 20
adding alternatives:[Oliver syndrome, Postaxial polydactyly - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2920]
processing orphanet number: 89839 ...  .. annotations: 6
NO OMIMENTRY FOR OMIM-ID 607600 creating NEW one
processing orphanet number: 89838 ...  .. annotations: 9
adding alternatives:[KRT14-related epidermolysis bullosa simplex, EBS-AR KRT14, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89838]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 70 ...  .. annotations: 17
processing orphanet number: 2929 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2928 ...  .. annotations: 17
processing orphanet number: 72 ...  .. annotations: 21
adding alternatives:[Angelman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=72]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 210122 ...  .. annotations: 23
adding alternatives:[Congenital alveolar capillary dysplasia, ACDMPV, Alveolar capillary dysplasia with misalignment of pulmonary veins, Alveolar capillary dysplasia with misalignment of pulmonary vessels, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=210122]
processing orphanet number: 2926 ...  .. annotations: 6
adding alternatives:[Polyneuropathy - hand defect, Hamanishi-Ueba-Tsuji syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2926]
processing orphanet number: 36426 ...  .. annotations: 42
NO OMIMENTRY FOR OMIM-ID 608579 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 2924 ...  .. annotations: 14
adding alternatives:[Isolated polycystic liver disease, ADPCLD, Autosomal dominant polycystic liver disease, PCLD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2924]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 77 ...  .. annotations: 29
processing orphanet number: 2930 ...  .. annotations: 44
adding alternatives:[Cronkhite-Canada syndrome, Gastrointestinal polyposis - ectodermal changes, Gastrointestinal polyposis - skin pigmentation - alopecia - fingernail changes, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2930]
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 80 ...  .. annotations: 39
  ... no hpo-term mapping for orphanet annotation: 35390
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 81 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 36412 ...  .. annotations: 49
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54840
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 83 ...  .. annotations: 30
adding alternatives:[Antley-Bixler syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=83]
processing orphanet number: 84 ...  .. annotations: 101
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1606 ...  .. annotations: 90
adding alternatives:[1p36 deletion syndrome, Del(1)(p36), Deletion 1p36, Deletion 1pter, Monosomy 1p36, Monosomy 1pter, Subtelomeric 1p36 deletion, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1606]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2935 ...  .. annotations: 11
NO OMIMENTRY FOR OMIM-ID 175690 creating NEW one
processing orphanet number: 87 ...  .. annotations: 45
adding alternatives:[Apert syndrome, ACS1, Acrocephalosyndactyly type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=87]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2934 ...  .. annotations: 30
adding alternatives:[Polysyndactyly - cardiac malformation, Bonneau syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2934]
processing orphanet number: 37748 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 324964 ...  .. annotations: 28
adding alternatives:[Chronic recurrent multifocal osteomyelitis, CRMO, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324964]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 157997 ...  .. annotations: 3
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 83628 ...  .. annotations: 16
processing orphanet number: 79133 ...  .. annotations: 15
adding alternatives:[Focal facial dermal dysplasia, FFDD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=398166, Focal facial dermal dysplasia type I, Bitemporal aplasia cutis congenita, Brauer syndrome, FFDD type I, FFDD1, Focal facial dermal dysplasia 1, Brauer type, Focal facial dermal dysplasia type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79133]
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 79132 ...  .. annotations: 7
processing orphanet number: 32960 ...  .. annotations: 48
adding alternatives:[Tumor necrosis factor receptor 1 associated periodic syndrome, Familial Hibernian fever, TNF receptor 1 associated periodic syndrome, TRAPS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=32960]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 2940 ...  .. annotations: 8
processing orphanet number: 90 ...  .. annotations: 9
adding alternatives:[Argininemia, Arginase deficiency, Hyperargininemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90]
processing orphanet number: 91 ...  .. annotations: 12
adding alternatives:[Aromatase deficiency, Congenital estrogen deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91]
processing orphanet number: 92 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 25750
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 93 ...  .. annotations: 41
adding alternatives:[Aspartylglucosaminuria, Aspartylglucosaminidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93]
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 96 ...  .. annotations: 26
adding alternatives:[Ataxia with vitamin E deficiency, AVED, Ataxia with isolated vitamin E deficiency, Familial isolated vitamin E deficiency, Friedreich-like ataxia, Isolated vitamin E deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=96]
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 2947 ...  .. annotations: 5
adding alternatives:[Triphalangeal thumbs - brachyectrodactyly, Carnevale-Hernández-del Castillo syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2947]
processing orphanet number: 2946 ...  .. annotations: 11
adding alternatives:[Brachydactyly - long thumb, Brachydactyly, long thumb type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2946]
processing orphanet number: 99 ...  .. annotations: 18
processing orphanet number: 83619 ...  .. annotations: 9
processing orphanet number: 2953 ...  .. annotations: 12
processing orphanet number: 1621 ...  .. annotations: 17
adding alternatives:[3q13 microdeletion syndrome, Del(3)(q13), Monosomy 3q13, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1621]
processing orphanet number: 2952 ...  .. annotations: 14
adding alternatives:[Adducted thumbs-arthrogryposis syndrome, Christian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2952]
processing orphanet number: 1620 ...  .. annotations: 35
adding alternatives:[Distal monosomy 3p, 3p- syndrome, Distal 3p deletion, Monosomy 3pter, Telomeric monosomy 3p, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1620]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2951 ...  .. annotations: 26
adding alternatives:[Absent thumb-short stature-immunodeficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2951]
processing orphanet number: 2950 ...  .. annotations: 11
adding alternatives:[Triphalangeal thumb - polysyndactyly syndrome, TPT-PS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2950, Polydactyly of a triphalangeal thumb, PPD2, Preaxial polydactyly type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93336]
processing orphanet number: 79129 ...  .. annotations: 4
processing orphanet number: 157991 ...  .. annotations: 1
processing orphanet number: 2959 ...  .. annotations: 34
adding alternatives:[Progeria - short stature - pigmented nevi, Mulvihill-Smith syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2959]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2958 ...  .. annotations: 31
adding alternatives:[X-linked intellectual disability - dysmorphism - cerebral atrophy, Prieto-Badia-Mulas syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2958]
  ... no hpo-term mapping for orphanet annotation: 3560
processing orphanet number: 2957 ...  .. annotations: 10
adding alternatives:[Guttmacher syndrome, Preaxial deficiency - postaxial polydactyly - hypospadias, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2957]
processing orphanet number: 2956 ...  .. annotations: 5
processing orphanet number: 171839 ...  .. annotations: 40
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 293355 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 171836 ...  .. annotations: 8
adding alternatives:[Amelogenesis imperfecta-gingival hyperplasia syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=171836]
processing orphanet number: 79152 ...  .. annotations: 8
processing orphanet number: 166002 ...  .. annotations: 12
processing orphanet number: 166011 ...  .. annotations: 10
adding alternatives:[Multiple epiphyseal dysplasia, Beighton type, Multiple epiphyseal dysplasia - myopia - deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166011]
processing orphanet number: 79156 ...  .. annotations: 3
adding alternatives:[Seizures - intellectual disability due to hydroxylysinuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79156]
processing orphanet number: 2964 ...  .. annotations: 4
adding alternatives:[Autosomal dominant prognathism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2964]
processing orphanet number: 2963 ...  .. annotations: 29
NO OMIMENTRY FOR OMIM-ID 612289 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2962 ...  .. annotations: 40
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2969 ...  .. annotations: 35
adding alternatives:[Cowden syndrome, Cowden disease, Multiple hamartoma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=201, Proteus-like syndrome, Cohen-Hayden syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2969, Lhermitte-Duclos disease, Dysplastic gangliocytoma of the cerebellum, LDD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=65285]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 2968 ...  .. annotations: 27
processing orphanet number: 1636 ...  .. annotations: 30
processing orphanet number: 95626 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 2980 ...  .. annotations: 52
adding alternatives:[Acro-oto-ocular syndrome, Pseudopapilledema - blepharophimosis - hand anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2980]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 56044 ...  .. annotations: 6
processing orphanet number: 79142 ...  .. annotations: 11
adding alternatives:[Familial Dupuytren contracture, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79142]
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 46240
  ... no hpo-term mapping for orphanet annotation: 40900
processing orphanet number: 79141 ...  .. annotations: 2
adding alternatives:[Hereditary painful callosities, Keratosis palmoplantaris nummularis, PPK nummularis, Plamoplantar hyperkeratosis nummularis, Plamoplantar keratoderma nummularis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79141]
processing orphanet number: 171829 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2976 ...  .. annotations: 19
adding alternatives:[Pseudoleprechaunism syndrome, Patterson type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2976]
processing orphanet number: 2975 ...  .. annotations: 6
adding alternatives:[46,XX disorder of sex development - skeletal anomalies, Female pseudohermaphroditism - skeletal anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2975]
processing orphanet number: 1643 ...  .. annotations: 12
processing orphanet number: 1642 ...  .. annotations: 27
processing orphanet number: 2973 ...  .. annotations: 15
processing orphanet number: 2972 ...  .. annotations: 8
adding alternatives:[Non-eruption of teeth - maxillary hypoplasia - genu valgum, Stoelinga-de Koomen-Davis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2972]
processing orphanet number: 2971 ...  .. annotations: 28
adding alternatives:[Peroxisomal acyl-CoA oxidase deficiency, Pseudo-NALD, Pseudo-neonatal adrenoleukodystrophy, Pseudoadrenoleukodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2971]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2970 ...  .. annotations: 34
adding alternatives:[Prune belly syndrome, Abdominal muscle deficiency syndrome, Eagle-Barret syndrome, Obrinsky syndrome, Triad Syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2970]
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1648 ...  .. annotations: 20
processing orphanet number: 1647 ...  .. annotations: 39
adding alternatives:[Oculocerebrocutaneous syndrome, Delleman syndrome, Delleman-Oorthuys syndrome, Leichtman-Wood-Rohn syndrome, OCCS, Orbital cyst with cerebral and focal dermal malformations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1647]
processing orphanet number: 2978 ...  .. annotations: 6
processing orphanet number: 93476 ...  .. annotations: 18
adding alternatives:[Mucopolysaccharidosis type 1, Alpha-L-iduronidase deficiency, MPS1, MPSI, Mucopolysaccharidosis type I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=579, Hurler-Scheie syndrome, MPS1H/S, MPSIH/S, Mucopolysaccharidosis type 1H/S, Mucopolysaccharidosis type IH/S, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93476]
processing orphanet number: 1660 ...  .. annotations: 16
adding alternatives:[Dermo-odonto dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1660]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 261304 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2990 ...  .. annotations: 64
adding alternatives:[Autosomal recessive multiple pterygium syndrome, Autosomal recessive non-lethal multiple pterygium syndrome, EVMPS, Escobar syndrome, Escobar variant multiple pterygium syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2990]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 93474 ...  .. annotations: 18
adding alternatives:[Mucopolysaccharidosis type 1, Alpha-L-iduronidase deficiency, MPS1, MPSI, Mucopolysaccharidosis type I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=579, Scheie syndrome, MPS1S, MPSIS, Mucopolysaccharidosis type 1S, Mucopolysaccharidosis type IS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93474]
processing orphanet number: 93473 ...  .. annotations: 58
adding alternatives:[Mucopolysaccharidosis type 1, Alpha-L-iduronidase deficiency, MPS1, MPSI, Mucopolysaccharidosis type I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=579, Hurler syndrome, Hurler disease, MPS1H, MPSIH, Mucopolysaccharidosis type 1H, Mucopolysaccharidosis type IH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93473]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1657 ...  .. annotations: 23
adding alternatives:[Dermatoosteolysis, Kirghizian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1657]
processing orphanet number: 2504 ...  .. annotations: 17
adding alternatives:[Metaphyseal dysplasia - maxillary hypoplasia - brachydacty, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2504]
processing orphanet number: 2988 ...  .. annotations: 17
adding alternatives:[Pterygium colli - intellectual disability - digital anomalies, Khalifa-Graham syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2988]
processing orphanet number: 1656 ...  .. annotations: 15
adding alternatives:[Dermatitis herpetiformis, Durhing-Brocq disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1656]
  ... no hpo-term mapping for orphanet annotation: 23330
processing orphanet number: 2987 ...  .. annotations: 22
adding alternatives:[Antecubital pterygium syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2987]
processing orphanet number: 2502 ...  .. annotations: 22
adding alternatives:[Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2502]
processing orphanet number: 1655 ...  .. annotations: 27
adding alternatives:[Müllerian derivatives - lymphangiectasia - polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1655]
  ... no hpo-term mapping for orphanet annotation: 24400
processing orphanet number: 1654 ...  .. annotations: 8
adding alternatives:[Natal teeth - intestinal pseudoobstruction - patent ductus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1654]
processing orphanet number: 2501 ...  .. annotations: 14
adding alternatives:[Metaphyseal chondrodysplasia, Spahr type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2501]
processing orphanet number: 2985 ...  .. annotations: 30
adding alternatives:[Pseudoprogeria syndrome, Eyebrows and eyelashes absence - intellectual disability, Hal-Berg-Rudolph syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2985]
processing orphanet number: 1653 ...  .. annotations: 5
processing orphanet number: 2500 ...  .. annotations: 19
NO OMIMENTRY FOR OMIM-ID 201200 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 2983 ...  .. annotations: 23
adding alternatives:[Disorder of sex development - intellectual disability, Pseudohermaphroditism - intellectual disability, Verloes-Gillerot-Fryns syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2983]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 2508 ...  .. annotations: 22
adding alternatives:[Microcephaly-corpus callosum agenesis-abnormal genitalia syndrome, Proud-Levine-Carpenter syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2508]
  ... no hpo-term mapping for orphanet annotation: 20340
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 1659 ...  .. annotations: 6
adding alternatives:[Dermatoleukodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1659]
processing orphanet number: 1658 ...  .. annotations: 10
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1235, Absence of fingerprints - congenital milia, Absence of dermatoglyphics - congenital milia, Baird syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1658]
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 2505 ...  .. annotations: 31
adding alternatives:[Multiple benign circumferential skin creases on limbs, CCSF, Congenital circumferential skin folds, Kunze-Riehm syndrome, MTBS, Michelin tire baby syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2505]
processing orphanet number: 2989 ...  .. annotations: 3
adding alternatives:[Pterygium of the conjunctiva, familial form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2989]
processing orphanet number: 1671 ...  .. annotations: 3
adding alternatives:[Diastematomyelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1671]
processing orphanet number: 2515 ...  .. annotations: 15
adding alternatives:[Microcephaly - cardiomyopathy, Winship-Viljoen-Leary syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2515]
processing orphanet number: 2999 ...  .. annotations: 4
adding alternatives:[Ptosis - strabismus - ectopic pupils, McPherson-Hall syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2999]
processing orphanet number: 79168 ...  .. annotations: 8
processing orphanet number: 1667 ...  .. annotations: 38
adding alternatives:[Wolcott-Rallison syndrome, Early-onset diabetes mellitus with multiple epiphyseal dysplasia, WRS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1667]
processing orphanet number: 2514 ...  .. annotations: 7
processing orphanet number: 2513 ...  .. annotations: 9
adding alternatives:[Microcephaly - albinism - digital anomalies, Castro Gago-Pombo-Novo syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2513]
processing orphanet number: 2997 ...  .. annotations: 7
adding alternatives:[Ptosis - vocal cord paralysis, Tucker syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2997]
processing orphanet number: 1665 ...  .. annotations: 8
processing orphanet number: 2511 ...  .. annotations: 28
adding alternatives:[Microbrachycephaly - ptosis - cleft lip, Richieri Costa-Guion Almeida-Ramos syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2511]
processing orphanet number: 2995 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1664 ...  .. annotations: 15
processing orphanet number: 2994 ...  .. annotations: 30
adding alternatives:[Short stature - craniofacial anomalies - genital hypoplasia, Haspeslagh-Fryns-Muelenaere syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2994]
processing orphanet number: 2510 ...  .. annotations: 39
processing orphanet number: 1662 ...  .. annotations: 40
adding alternatives:[Restrictive dermopathy, Hyperkeratosis-contracture syndrome, Lethal restrictive dermopathy, Tight skin contracture syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1662]
processing orphanet number: 1661 ...  .. annotations: 5
adding alternatives:[X-linked corneal dermoid, Corneal dystrophy epithelial - short stature, Guízar Vázquez-Luengas-Muñoz syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1661]
processing orphanet number: 284400 ...  .. annotations: 6
processing orphanet number: 2519 ...  .. annotations: 24
processing orphanet number: 2518 ...  .. annotations: 23
processing orphanet number: 2516 ...  .. annotations: 23
adding alternatives:[Microcephaly - cardiac defect - lung malsegmentation, Ellis-Yale-Winter syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2516]
processing orphanet number: 157973 ...  .. annotations: 25
adding alternatives:[Congenital muscular dystrophy due to LMNA mutation, L-CMD, LMNA-related congenital muscular dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157973]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1682 ...  .. annotations: 3
adding alternatives:[Arterial dissection - lentiginosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1682]
processing orphanet number: 1681 ...  .. annotations: 9
processing orphanet number: 1680 ...  .. annotations: 6
adding alternatives:[Spastic diplegia, infantile type, Little syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1680]
processing orphanet number: 35173 ...  .. annotations: 28
adding alternatives:[X-linked dominant chondrodysplasia punctata, CDPX2, CDPXD, CPXD, Chondrodystrophia calcificans congenita, Conradi-Hünermann-Happle syndrome, X-linked chondrodysplasia punctata type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35173]
processing orphanet number: 2526 ...  .. annotations: 48
adding alternatives:[Microcephaly - lymphedema - chorioretinopathy, MLCRD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2526]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2523 ...  .. annotations: 7
processing orphanet number: 2522 ...  .. annotations: 25
adding alternatives:[Microcephaly - cervical spine fusion anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2522]
processing orphanet number: 168624 ...  .. annotations: 16
adding alternatives:[Familial scaphocephaly syndrome, McGillivray type, Scaphocephaly - macrocephaly - maxillary retrusion - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168624]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 2521 ...  .. annotations: 8
processing orphanet number: 1672 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2528 ...  .. annotations: 15
processing orphanet number: 157965 ...  .. annotations: 19
adding alternatives:[Ehlers-Danlos syndrome, spondylocheirodysplastic type, EDS, spondylocheirodysplastic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157965]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 41842 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 43430
processing orphanet number: 2536 ...  .. annotations: 11
adding alternatives:[Microcornea - glaucoma - absent frontal sinuses, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2536]
processing orphanet number: 2535 ...  .. annotations: 6
processing orphanet number: 1203 ...  .. annotations: 5
adding alternatives:[Duodenal atresia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1203]
processing orphanet number: 1202 ...  .. annotations: 8
adding alternatives:[Larynx atresia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1202]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2533 ...  .. annotations: 14
adding alternatives:[Microcephaly - deafness - intellectual disability, Kawashima-Tsuji syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2533]
processing orphanet number: 1685 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1200 ...  .. annotations: 12
adding alternatives:[Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome, Burn-McKeown syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1200]
processing orphanet number: 1208 ...  .. annotations: 6
adding alternatives:[Pulmonary atresia - intact ventricular septum, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1208]
processing orphanet number: 2538 ...  .. annotations: 34
adding alternatives:[Microgastria - limb reduction defect, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2538]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 261344 ...  .. annotations: 43
processing orphanet number: 2551 ...  .. annotations: 27
adding alternatives:[Microspherophakia - metaphyseal dysplasia, Verloes-Van Maldergem-de Marneffe syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2551]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 261349 ...  .. annotations: 74
adding alternatives:[2p15p16.1 microdeletion syndrome, 2p15-p16.1 microdeletion syndrome, Del(2)(p15p16.1), Monosomy 2p15-p16.1, Monosomy 2p15p16.1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261349]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1216 ...  .. annotations: 5
adding alternatives:[Autosomal dominant congenital benign spinal muscular atrophy, Autosomal dominant benign distal spinal muscular atrophy, Congenital benign spinal muscular atrophy with contractures, Congenital nonprogressive spinal muscular atrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1216]
processing orphanet number: 2547 ...  .. annotations: 15
processing orphanet number: 1699 ...  .. annotations: 30
processing orphanet number: 1215 ...  .. annotations: 10
processing orphanet number: 1214 ...  .. annotations: 11
adding alternatives:[Progressive hemifacial atrophy, Hemifacial atrophy, PHA, Parry-Romberg syndrome, Progressive facial hemiatrophy, Romberg syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1214]
processing orphanet number: 1695 ...  .. annotations: 24
processing orphanet number: 2549 ...  .. annotations: 33
adding alternatives:[Oculoauriculovertebral spectrum with radial defects, Hemifacial microsomia - radial defects, Moeschler-Clarren syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2549]
processing orphanet number: 261330 ...  .. annotations: 60
adding alternatives:[Distal 22q11.2 microdeletion syndrome, Distal del(22)(q11.2), Distal monosomy 22q11.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261330]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1231 ...  .. annotations: 26
adding alternatives:[Barber-Say syndrome, Hypertrichosis - atrophic skin - ectropion - macrostomia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1231]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 261337 ...  .. annotations: 57
processing orphanet number: 2561 ...  .. annotations: 14
adding alternatives:[Ackerman syndrome, Pyramidal molar - glaucoma - upper abnormal lip, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2561]
processing orphanet number: 1228 ...  .. annotations: 5
adding alternatives:[Banki syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1228]
processing orphanet number: 3406 ...  .. annotations: 8
NO OMIMENTRY FOR OMIM-ID 604093 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23490
processing orphanet number: 1227 ...  .. annotations: 22
adding alternatives:[Bangstad syndrome, Ataxia - diabetes - goiter - gonadal insufficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1227]
processing orphanet number: 2558 ...  .. annotations: 21
processing orphanet number: 3405 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 35701 ...  .. annotations: 5
NO OMIMENTRY FOR OMIM-ID 605911 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 1226 ...  .. annotations: 10
adding alternatives:[Bamforth-Lazarus syndrome, Athyroidal hypothyroidism-spiky hair-cleft palate syndrome, Bamforth syndrome, Hypothyroidism - cleft palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1226]
processing orphanet number: 2557 ...  .. annotations: 24
adding alternatives:[Mietens syndrome, Intellectual disability, Mietens-Weber type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2557]
processing orphanet number: 3404 ...  .. annotations: 25
adding alternatives:[Ulbright-Hodes syndrome, Renal dysplasia - limb defects, Renal dysplasia - mesomelia - radiohumeral fusion, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3404]
processing orphanet number: 1225 ...  .. annotations: 43
adding alternatives:[Baller-Gerold syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1225]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2556 ...  .. annotations: 51
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3403 ...  .. annotations: 4
adding alternatives:[Uhl anomaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3403, Familial isolated arrhythmogenic right ventricular dysplasia, Familial isolated ARVC, Familial isolated ARVD, Familial isolated arrhythmogenic right ventricular cardiomyopathy, Familial isolated arrhythmogenic ventricular cardiomyopathy, Familial isolated arrhythmogenic ventricular dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=217656]
processing orphanet number: 2554 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 1221 ...  .. annotations: 6
adding alternatives:[Cheilitis glandularis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1221]
processing orphanet number: 800 ...  .. annotations: 106
adding alternatives:[Schwartz-Jampel syndrome, Aberfeld syndrome, Burton disease, Burton skeletal dysplasia, Burton syndrome, Catel-Hempel syndrome, Dysostosis enchondralis metaepiphysaria, Catel-Hempel type, Myotonic chondrodystrophy, Myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies, Osteochondromuscular dystrophy, SJS, SJS1, Schwartz-Jampel syndrome type 1, Schwartz-Jampel-Aberfeld syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=800]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 100100 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 801 ...  .. annotations: 79
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 805 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 23710
  ... no hpo-term mapping for orphanet annotation: 23740
processing orphanet number: 3409 ...  .. annotations: 30
adding alternatives:[Urban-Rogers-Meyer syndrome, Intellectual disability - short stature - hand contractures - genital anomalies, Prader-Willi habitus - osteopenia - camptodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3409]
processing orphanet number: 3408 ...  .. annotations: 7
adding alternatives:[Upington disease, Hip dysplasia - enchondromata - ecchondroma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3408]
processing orphanet number: 1229 ...  .. annotations: 8
adding alternatives:[Congenital intrauterine infection-like syndrome, BLC-PMG, Baraitser-Brett-Piesowicz syndrome, Baraitser-Reardon syndrome, Bilateral band-like calcification with polymicrogyria, Microcephaly - intracranial calcification - intellectual disability, Pseudo-TORCH syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1229]
processing orphanet number: 808 ...  .. annotations: 24
processing orphanet number: 809 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 2573 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 1241 ...  .. annotations: 8
adding alternatives:[Bencze syndrome, Hemifacial hyperplasia - strabismus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1241]
processing orphanet number: 2572 ...  .. annotations: 12
adding alternatives:[Spastic ataxia - corneal dystrophy, Bedouin spastic ataxia syndrome, Mousa-Al Din-Al Nassar syndrome, Spastic ataxia - ocular anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2572]
processing orphanet number: 1240 ...  .. annotations: 24
adding alternatives:[Metaphyseal acroscyphodysplasia, Bellini syndrome, Intellectual disability - short stature - wedge shaped epiphyses of knees, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1240]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 2571 ...  .. annotations: 13
adding alternatives:[X-linked immunoneurologic disorder, Woods-Black-Norbury syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2571]
processing orphanet number: 2570 ...  .. annotations: 25
adding alternatives:[Holoprosencephaly-hypokinesia-congenital contractures syndrome, Holoprosencephaly-fetal akinesia/hypokinesia sequence syndrome, Morse-Rawnsley-Sargent syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2570]
processing orphanet number: 1239 ...  .. annotations: 9
adding alternatives:[Behr syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1239]
processing orphanet number: 3417 ...  .. annotations: 13
adding alternatives:[Van den Bosch syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3417]
processing orphanet number: 228302 ...  .. annotations: 8
adding alternatives:[Carnitine palmitoyltransferase II deficiency, CPT2, CPTII, Carnitine palmitoyltransferase deficiency type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157, Carnitine palmitoyl transferase II deficiency, myopathic form, CPT2, adult-onset form, CPT2, myopathic form, CPTII, adult-onset form, CPTII, myopathic form, Carnitine palmitoyl transferase II deficiency, adult-onset form, Carnitine palmitoyl transferase deficiency type 2, adult-onset form, Carnitine palmitoyl transferase deficiency type 2, myopathic form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228302]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 3416 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 1237 ...  .. annotations: 15
adding alternatives:[Beemer-Ertbruggen syndrome, Hydrocephalus - cardiac malformation - dense bones, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1237]
processing orphanet number: 251510 ...  .. annotations: 9
processing orphanet number: 1236 ...  .. annotations: 33
processing orphanet number: 79312 ...  .. annotations: 29
adding alternatives:[Vitamin B12-unresponsive methylmalonic acidemia, Vitamin B12-unresponsive methylmalonic aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=27, Vitamin B12-unresponsive methylmalonic acidemia type mut0, Complete deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut0, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=289916, Vitamin B12-unresponsive methylmalonic acidemia type mut-, Partial deficiency of methylmalonyl-CoA mutase, Vitamin B12-unresponsive methylmalonic aciduria type mut-, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79312]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1234 ...  .. annotations: 28
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1234]
processing orphanet number: 2565 ...  .. annotations: 20
adding alternatives:[Mononen-Karnes-Senac syndrome, Skeletal dysplasia - brachydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2565]
processing orphanet number: 3412 ...  .. annotations: 29
processing orphanet number: 79314 ...  .. annotations: 12
adding alternatives:[L-2-hydroxyglutaric aciduria, L-2-HGA, L-2-hydroxyglutaric acidemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79314]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2564 ...  .. annotations: 2
adding alternatives:[Tetramelic monodactyly, Sommer-Hines syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2564]
processing orphanet number: 3411 ...  .. annotations: 9
adding alternatives:[Double uterus - hemivagina - renal agenesis, Double uterus and obstructed hemivagina syndrome, Herlyn-Werner syndrome, OHVIRA syndrome, Obstructed hemivagina and ipsilateral renal anomaly, Wunderlich syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3411]
processing orphanet number: 1232 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 2563 ...  .. annotations: 14
adding alternatives:[MOMO syndrome, Macrocephaly-obesity-mental disability-ocular abnormalities syndrome, Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2563]
processing orphanet number: 811 ...  .. annotations: 28
adding alternatives:[Shwachman-Diamond syndrome, Pancreatic insufficiency and bone marrow dysfunction, SDS, Shwachman syndrome, Shwachman-Bodian-Diamond syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=811]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79319 ...  .. annotations: 5
adding alternatives:[MPI-CDG, CDG syndrome type Ib, CDG-Ib, CDG1B, Carbohydrate deficient glycoprotein syndrome type Ib, Congenital disorder of glycosylation type 1b, Congenital disorder of glycosylation type Ib, Phosphomannose isomerase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79319]
processing orphanet number: 812 ...  .. annotations: 40
adding alternatives:[Sialidosis type 1, Cherry-red spot-myoclonus syndrome, Lipomucopolysaccharidosis, Normomorphic sialidosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=812, Sialidosis type 2, Infantile dysmorphic sialidosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=87876]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 49500
processing orphanet number: 813 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 816 ...  .. annotations: 29
adding alternatives:[Sjögren-Larsson syndrome, Fatty acid alcohol oxidoreductase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=816]
processing orphanet number: 156177 ...  .. annotations: 32
processing orphanet number: 3419 ...  .. annotations: 37
processing orphanet number: 817 ...  .. annotations: 7
processing orphanet number: 818 ...  .. annotations: 106
adding alternatives:[Smith-Lemli-Opitz syndrome, 7-dehydrocholesterol reductase deficiency, RSH syndrome, SLOS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=818]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 819 ...  .. annotations: 72
adding alternatives:[Smith-Magenis syndrome, 17p11.2 microdeletion syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=819]
  ... no hpo-term mapping for orphanet annotation: 26020
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 238578 ...  .. annotations: 5
adding alternatives:[Familial clubfoot with or without associated lower limb anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=199315, Familial clubfoot due to 17q23.1q23.2 microduplication, Hereditary clubfoot due to 17q23.1-q23.2 microduplication, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238578]
processing orphanet number: 1253 ...  .. annotations: 12
adding alternatives:[Ascher syndrome, Blepharochalasis - double lip, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1253]
processing orphanet number: 2584 ...  .. annotations: 23
adding alternatives:[Classic mycosis fungoides, Mycosis fungoides, Alibert-Bazin type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2584]
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 1252 ...  .. annotations: 30
adding alternatives:[Blepharonasofacial malformation syndrome, Pashayan syndrome, Pashayan-Prozansky syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1252]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 2582 ...  .. annotations: 10
processing orphanet number: 2580 ...  .. annotations: 15
processing orphanet number: 261318 ...  .. annotations: 66
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1248 ...  .. annotations: 22
adding alternatives:[Maxillonasal dysplasia, Binder syndrome, Maxillonasal dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1248]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 55480
processing orphanet number: 2579 ...  .. annotations: 4
adding alternatives:[Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus, Furukawa-Takagi-Nakao syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2579]
processing orphanet number: 79302 ...  .. annotations: 11
adding alternatives:[Congenital bile acid synthesis defect type 3, Oxysterol 7-alpha-hydroxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79302]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2578 ...  .. annotations: 11
adding alternatives:[Mayer-Rokitansky-Küster-Hauser syndrome type 2, Atypical MRKH syndrome, MRKH syndrome type 2, MURCS association, Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2578, Mayer-Rokitansky-Küster-Hauser syndrome, MRKH syndrome, Rokitansky syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3109]
processing orphanet number: 79301 ...  .. annotations: 17
adding alternatives:[Congenital bile acid synthesis defect type 1, 3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79301]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3424 ...  .. annotations: 19
adding alternatives:[Velo-facial-skeletal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3424]
  ... no hpo-term mapping for orphanet annotation: 55720
processing orphanet number: 1246 ...  .. annotations: 16
adding alternatives:[Brachydactyly - nystagmus - cerebellar ataxia, Biemond syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1246]
processing orphanet number: 2576 ...  .. annotations: 9
adding alternatives:[MULIBREY nanism, MULIBREY dwarfism, Muscle-liver-brain-eye nanism, Perheentupa syndrome, Pericardial constriction - growth failure, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2576]
processing orphanet number: 79303 ...  .. annotations: 12
adding alternatives:[Congenital bile acid synthesis defect type 2, Cholestasis, with delta(4)-3-oxosteroid 5-beta-reductase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79303]
processing orphanet number: 2575 ...  .. annotations: 17
adding alternatives:[Cystic fibrosis - gastritis - megaloblastic anemia, Lubani-Al Saleh-Teebi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2575]
processing orphanet number: 820 ...  .. annotations: 24
adding alternatives:[Sneddon syndrome, Ehrmann-Sneddon syndrome, Livedo racemosa and cerebrovascular accidents, Livedo reticularis and cerebrovascular accidents, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=820]
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 821 ...  .. annotations: 47
adding alternatives:[Sotos syndrome, Cerebral gigantism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=821]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2574 ...  .. annotations: 11
adding alternatives:[Moynahan syndrome, Alopecia-epilepsy-oligophrenia syndrome, Moynahan type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2574]
processing orphanet number: 3421 ...  .. annotations: 10
adding alternatives:[Retinal vasculopathy and cerebral leukodystrophy, RVCL, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=247691, Cerebroretinal vasculopathy, CRV, Grand-Kaine-Fulling syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3421, HERNS syndrome, Hereditary endotheliopathy - retinopathy - nephropathy - stroke, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=63261, Hereditary vascular retinopathy, HVR, Hereditary vascular retinopathy - Raynaud phenomenon - migraine, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=71291]
processing orphanet number: 1243 ...  .. annotations: 6
adding alternatives:[Best vitelliform macular dystrophy, BMD, BVMD, Best disease, Best macular dystrophy, Early-onset vitelliform macular dystrophy, Juvenile-onset vitelliform macular dystrophy, Polymorphic vitelline macular degeneration, Vitelliform macular dystrophy type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1243]
processing orphanet number: 823 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 825 ...  .. annotations: 43
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 828 ...  .. annotations: 67
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3429 ...  .. annotations: 20
adding alternatives:[Verloove Vanhorick-Brubakk syndrome, Cleft - limb-heart malformation syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3429]
processing orphanet number: 829 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 1264 ...  .. annotations: 10
adding alternatives:[Tricho-retino-dento-digital syndrome, Bork syndrome, Uncombable hair - retinal pigmentary dystrophy - dental anomalies - brachydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1264]
processing orphanet number: 2111 ...  .. annotations: 5
processing orphanet number: 1263 ...  .. annotations: 21
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1263]
processing orphanet number: 2110 ...  .. annotations: 3
adding alternatives:[Hallux varus - preaxial polysyndactyly, Kleiner-Holmes syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2110]
processing orphanet number: 3440 ...  .. annotations: 30
processing orphanet number: 1262 ...  .. annotations: 11
adding alternatives:[Böök syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1262]
processing orphanet number: 1261 ...  .. annotations: 11
adding alternatives:[Bonnemann-Meinecke-Reich syndrome, Encephalopathy - intracerebral calcification - retinal degeneration, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1261]
processing orphanet number: 2591 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 45510
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 2590 ...  .. annotations: 8
adding alternatives:[Hereditary myoclonus - progressive distal muscular atrophy, Jankovic-Rivera syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2590]
processing orphanet number: 79330 ...  .. annotations: 3
adding alternatives:[GCS1-CDG, CDG syndrome type IIb, CDG-IIb, CDG2B, Carbohydrate deficient glycoprotein syndrome type IIb, Congenital disorder of glycosylation type 2b, Congenital disorder of glycosylation type IIb, Glucosidase 1 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79330]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2108 ...  .. annotations: 52
adding alternatives:[Hallermann-Streiff syndrome, François dyscephalic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2108]
processing orphanet number: 3439 ...  .. annotations: 13
adding alternatives:[Von Voss-Cherstvoy syndrome, DK phocomelia syndrome, Phocomelia - thrombocytopenia - encephalocele - urogenital malformations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3439]
processing orphanet number: 79333 ...  .. annotations: 3
NO OMIMENTRY FOR OMIM-ID 608779 creating NEW one
processing orphanet number: 2107 ...  .. annotations: 28
adding alternatives:[Hall-Riggs syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2107]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79332 ...  .. annotations: 5
adding alternatives:[B4GALT1-CDG, Beta-1,4-galactosyltransferase deficiency, CDG syndrome type IId, CDG-IId, CDG2D, Carbohydrate deficient glycoprotein syndrome type IId, Congenital disorder of glycosylation type 2d, Congenital disorder of glycosylation type IId, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79332]
processing orphanet number: 1259 ...  .. annotations: 11
adding alternatives:[Blepharoptosis - myopia - ectopia lentis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1259]
processing orphanet number: 3437 ...  .. annotations: 13
processing orphanet number: 2589 ...  .. annotations: 9
adding alternatives:[Myoclonus-cerebellar ataxia-deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2589]
processing orphanet number: 1258 ...  .. annotations: 6
processing orphanet number: 2104 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 3560
processing orphanet number: 2588 ...  .. annotations: 35
adding alternatives:[Myhre syndrome, Facial dysmorphism - intellectual disability - short stature - hearing loss, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2588]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 1256 ...  .. annotations: 25
processing orphanet number: 3434 ...  .. annotations: 12
adding alternatives:[MMEP syndrome, MCOPS8, Microcephaly - microphthalmia - ectrodactyly of lower limbs - prognathism, Syndromic microphthalmia type 8, Viljoen-Smart syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3434]
  ... no hpo-term mapping for orphanet annotation: 52000
processing orphanet number: 830 ...  .. annotations: 2
processing orphanet number: 275543 ...  .. annotations: 17
processing orphanet number: 3433 ...  .. annotations: 17
processing orphanet number: 2101 ...  .. annotations: 15
adding alternatives:[Grubben-de Cock-Borghgraef syndrome, Developmental delay - hypotonia - extremities hypertrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2101]
processing orphanet number: 2585 ...  .. annotations: 16
adding alternatives:[Ataxia - pancytopenia, Myelocerebellar disorder, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2585]
processing orphanet number: 833 ...  .. annotations: 22
processing orphanet number: 834 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 839 ...  .. annotations: 4
adding alternatives:[Congenital nephrotic syndrome, Finnish type, Finnish congenital nephrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=839]
processing orphanet number: 137831 ...  .. annotations: 20
adding alternatives:[X-linked intellectual disability - cerebellar hypoplasia, OPHN1 syndrome, Oligophrenin-1 syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=137831]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1275 ...  .. annotations: 12
adding alternatives:[Brachydactyly - elbow wrist dysplasia, Brachydactyly - joint dysplasia, Liebenberg syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1275]
processing orphanet number: 3453 ...  .. annotations: 15
adding alternatives:[Autoimmune polyendocrinopathy type 1, APECED syndrome, APS type 1, APS1, Autoimmune hypoparathyroidism - chronic candidiasis - Addison's disease, Autoimmune hypoparathyroidism - chronic candidosis - Addison's disease, Autoimmune polyendocrine syndrome type 1, Autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy syndrome, Autoimmune polyendocrinopathy - candidosis - ectodermal dystrophy syndrome, Autoimmune polyglandular syndrome type 1, HAM syndrome, Hypoparathyroidism - Addison's disease - mucocutaneous candidiasis, Hypoparathyroidism - Addison's disease - mucocutaneous candidosis, MEDAC syndrome, Multiple endocrine deficiency - Addison's disease - candidiasis, Multiple endocrine deficiency - Addison's disease - candidosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3453]
processing orphanet number: 3452 ...  .. annotations: 45
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 1272 ...  .. annotations: 44
adding alternatives:[Fine-Lubinsky syndrome, Brachycephaly - deafness - cataract - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1272]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1270 ...  .. annotations: 20
adding alternatives:[Bowen-Conradi syndrome, Bowen syndrome, Hutterite type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1270]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 228305 ...  .. annotations: 9
adding alternatives:[Carnitine palmitoyltransferase II deficiency, CPT2, CPTII, Carnitine palmitoyltransferase deficiency type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157, Carnitine palmitoyl transferase II deficiency, severe infantile form, CPT2, hepatocardiomuscular form, CPT2, severe infantile form, CPTII, hepatocardiomuscular form, CPTII, severe infantile form, Carnitine palmitoyl transferase II deficiency, hepatocardiomuscular form, Carnitine palmitoyl transferase deficiency type 2, hepatocardiomuscular form, Carnitine palmitoyl transferase deficiency type 2, severe infantile form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228305]
processing orphanet number: 228308 ...  .. annotations: 12
adding alternatives:[Carnitine palmitoyltransferase II deficiency, CPT2, CPTII, Carnitine palmitoyltransferase deficiency type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157, Carnitine palmitoyl transferase II deficiency, neonatal form, CPT2, lethal systemic form, CPT2, neonatal form, CPTII, lethal systemic form, CPTII, neonatal form, Carnitine palmitoyl transferase II deficiency, lethal systemic form, Carnitine palmitoyl transferase deficiency type 2, lethal systemic form, Carnitine palmitoyl transferase deficiency type 2, neonatal form, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228308]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79320 ...  .. annotations: 3
adding alternatives:[ALG6-CDG, CDG syndrome type Ic, CDG-Ic, CDG1C, Carbohydrate deficient glycoprotein syndrome type Ic, Congenital disorder of glycosylation type 1c, Congenital disorder of glycosylation type Ic, Glucosyltransferase 1 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79320]
processing orphanet number: 2119 ...  .. annotations: 13
adding alternatives:[HEC syndrome, Hydrocephalus - endocardial fibroelastosis - cataract, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2119]
  ... no hpo-term mapping for orphanet annotation: 55720
processing orphanet number: 79322 ...  .. annotations: 5
adding alternatives:[DPM1-CDG, CDG syndrome type Ie, CDG-Ie, CDG1E, Carbohydrate deficient glycoprotein syndrome type Ie, Congenital disorder of glycosylation type 1e, Congenital disorder of glycosylation type Ie, Dol-P-mannosyltransferase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79322]
processing orphanet number: 2118 ...  .. annotations: 7
adding alternatives:[Hawkinsinuria, 4-HPPD deficiency, 4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, 4-hydroxyphenylpyruvic acid dioxygenase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2118]
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3449 ...  .. annotations: 19
processing orphanet number: 228312 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79321 ...  .. annotations: 5
adding alternatives:[ALG3-CDG, CDG syndrome type Id, CDG-Id, CDG1D, Carbohydrate deficient glycoprotein syndrome type Id, Congenital disorder of glycosylation type 1d, Congenital disorder of glycosylation type Id, Mannosyltransferase 6 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79321]
processing orphanet number: 168555 ...  .. annotations: 9
adding alternatives:[Spondylometaphyseal dysplasia, A4 type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168555]
processing orphanet number: 2117 ...  .. annotations: 21
adding alternatives:[Hartsfield-Bixler-Demyer syndrome, Holoprosencephaly - ectrodactyly - cleft lip palate, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2117]
processing orphanet number: 3448 ...  .. annotations: 29
processing orphanet number: 79324 ...  .. annotations: 4
NO OMIMENTRY FOR OMIM-ID 607143 creating NEW one
processing orphanet number: 2116 ...  .. annotations: 26
adding alternatives:[Hartnup disease, Aminoaciduria, Hartnup type, Hartnup disorder, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2116]
processing orphanet number: 3447 ...  .. annotations: 37
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3447]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79323 ...  .. annotations: 4
adding alternatives:[MPDU1-CDG, CDG syndrome type If, CDG-If, CDG1F, Carbohydrate deficient glycoprotein syndrome type If, Congenital disorder of glycosylation type 1f, Congenital disorder of glycosylation type If, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79323]
processing orphanet number: 2115 ...  .. annotations: 26
adding alternatives:[Harrod syndrome, Cranio-facio-digito-genital syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2115]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 840 ...  .. annotations: 6
processing orphanet number: 79326 ...  .. annotations: 5
adding alternatives:[ALG2-CDG, CDG syndrome type Ii, CDG-Ii, CDG1I, Carbohydrate deficient glycoprotein syndrome type Ii, Congenital disorder of glycosylation type 1i, Congenital disorder of glycosylation type Ii, Mannosyltransferase 2 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79326]
processing orphanet number: 1267 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2598 ...  .. annotations: 17
processing orphanet number: 2114 ...  .. annotations: 9
adding alternatives:[Hip dysplasia, Beukes type, BFHD, Beukes familial hip dysplasia, Cilliers-Beighton syndrome, Premature degenerative osteoarthropathy of the hip, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2114]
processing orphanet number: 841 ...  .. annotations: 4
adding alternatives:[Sebocystomatosis, Steatocystoma multiplex, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=841]
processing orphanet number: 79325 ...  .. annotations: 4
NO OMIMENTRY FOR OMIM-ID 608104 creating NEW one
processing orphanet number: 2597 ...  .. annotations: 9
adding alternatives:[Mitochondrial myopathy - lactic acidosis - deafness, Mitochondrial myopathy - lactic acidosis - hearing loss, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2597]
processing orphanet number: 1266 ...  .. annotations: 35
adding alternatives:[Dermato-cardio-skeletal syndrome, Borrone type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1266]
processing orphanet number: 79328 ...  .. annotations: 4
NO OMIMENTRY FOR OMIM-ID 608776 creating NEW one
processing orphanet number: 79327 ...  .. annotations: 8
adding alternatives:[ALG1-CDG, CDG syndrome type Ik, CDG-Ik, CDG1K, Carbohydrate deficient glycoprotein syndrome type Ik, Congenital disorder of glycosylation type 1k, Congenital disorder of glycosylation type Ik, Mannosyltransferase 1 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79327]
processing orphanet number: 845 ...  .. annotations: 22
adding alternatives:[Tay-Sachs disease, GM2 gangliosidosis, B, B1 variant, Hexosaminidase A deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=845]
  ... no hpo-term mapping for orphanet annotation: 49500
processing orphanet number: 79329 ...  .. annotations: 2
adding alternatives:[MGAT2-CDG, CDG syndrome type IIa, CDG-IIa, CDG2A, Carbohydrate deficient glycoprotein syndrome type IIa, Congenital disorder of glycosylation type 2a, Congenital disorder of glycosylation type IIa, N-acetylglucosaminyltransferase 2 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79329]
processing orphanet number: 846 ...  .. annotations: 13
adding alternatives:[Alpha-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=846]
processing orphanet number: 847 ...  .. annotations: 55
adding alternatives:[Alpha-thalassemia-X-linked intellectual disability syndrome, ATR-X syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=847]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 848 ...  .. annotations: 23
adding alternatives:[Beta-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=848, Beta-thalassemia intermedia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231222, Beta-thalassemia major, Cooley anemia, Mediterranean anemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231214]
processing orphanet number: 3464 ...  .. annotations: 8
adding alternatives:[Woodhouse-Sakati syndrome, Diabetes - hypogonadism - deafness - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3464]
processing orphanet number: 3463 ...  .. annotations: 49
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2130 ...  .. annotations: 8
processing orphanet number: 168593 ...  .. annotations: 19
adding alternatives:[Sudden infant death - dysgenesis of the testes, SIDDT, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168593]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3460 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 20160
processing orphanet number: 2128 ...  .. annotations: 14
adding alternatives:[Isolated hemihyperplasia, Hemi 3 syndrome, Hemicorporal hypertrophy, Isolated hemihypertrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2128]
processing orphanet number: 3459 ...  .. annotations: 38
adding alternatives:[Wilson-Turner syndrome, X-linked intellectual disability - gynecomastia - obesity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3459]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 79357 ...  .. annotations: 4
processing orphanet number: 851 ...  .. annotations: 2
adding alternatives:[Paris-Trousseau thrombocytopenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=851]
processing orphanet number: 1278 ...  .. annotations: 12
adding alternatives:[Brachydactyly - preaxial hallux varus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1278]
processing orphanet number: 3456 ...  .. annotations: 12
adding alternatives:[Wildervanck syndrome, Cervico-oculo-acoustic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3456]
processing orphanet number: 79358 ...  .. annotations: 8
processing orphanet number: 2124 ...  .. annotations: 5
adding alternatives:[Cavernous hemangiomas of face - supraumbilical midline raphe, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2124]
processing orphanet number: 3455 ...  .. annotations: 35
adding alternatives:[Wiedemann-Rautenstrauch syndrome, Neonatal progeroid syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3455]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1277 ...  .. annotations: 11
processing orphanet number: 1276 ...  .. annotations: 6
adding alternatives:[Brachydactyly-arterial hypertension syndrome, Bilginturan brachydactyly, Bilginturan syndrome, Brachydactyly, type E, with short stature and hypertension, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1276]
processing orphanet number: 2123 ...  .. annotations: 21
processing orphanet number: 3454 ...  .. annotations: 13
adding alternatives:[Intellectual disability-developmental delay-contractures syndrome, Foot contractures-muscle atrophy-oculomotor apraxia, Wieacker-Wolff syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3454]
processing orphanet number: 183707 ...  .. annotations: 2
adding alternatives:[Neutrophil immunodeficiency syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=183707]
processing orphanet number: 856 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 857 ...  .. annotations: 60
adding alternatives:[Townes-Brocks syndrome, Imperforate anus with hand, foot and ear anomalies, REAR syndrome, Renal-ear-anal-radial syndrome, Sensorineural deafness with imperforate anus and hypoplastic thumbs, TBS, Townes syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=857]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 858 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 55200
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 859 ...  .. annotations: 9
adding alternatives:[Transcobalamin deficiency, Inherited deficiency of transcobalamin, Transcobalamin II deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=859]
  ... no hpo-term mapping for orphanet annotation: 52600
processing orphanet number: 178382 ...  .. annotations: 1
adding alternatives:[Congenital vertical talus, Congenital convex foot, Congenital convex pes valgus, Congenital rocker-bottom foot, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178382]
processing orphanet number: 183713 ...  .. annotations: 5
NO OMIMENTRY FOR OMIM-ID 612260 creating NEW one
processing orphanet number: 1297 ...  .. annotations: 37
adding alternatives:[Branchio-oculo-facial syndrome, BOFS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1297]
processing orphanet number: 1296 ...  .. annotations: 17
adding alternatives:[Lambert syndrome, Branchial dysplasia - intellectual disability - inguinal hernia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1296]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2143 ...  .. annotations: 29
adding alternatives:[Donnai-Barrow syndrome, DBS/FOAR syndrome, Diaphragmatic hernia-exomphalos-hypertelorism syndrome, Diaphragmatic hernia-hypertelorism-myopia-deafness syndrome, FOAR syndrome, Facio-oculo-acoustico-renal syndrome, Holmes-Schepens syndrome, Syndrome of ocular and facial anomalies, telecanthus and deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2143]
processing orphanet number: 3474 ...  .. annotations: 48
adding alternatives:[CHIME syndrome, Coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome, Congenital disorder of glycosylation due to PIGL deficiency, Neuroectodermal dysplasia, CHIME type, Neuroectodermal syndrome, Zunich type, PIGL-CDG, Zunich-Kaye syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3474]
processing orphanet number: 1295 ...  .. annotations: 20
adding alternatives:[Brachytelephalangy - dysmorphism - Kallmann syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1295]
processing orphanet number: 3473 ...  .. annotations: 40
processing orphanet number: 2141 ...  .. annotations: 17
adding alternatives:[Diaphragmatic defect - limb deficiency - skull defect, Froster-Huch syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2141]
processing orphanet number: 3472 ...  .. annotations: 66
adding alternatives:[Yunis-Varon syndrome, Cleidocranial dysplasia - micrognathia - absent thumbs, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3472]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2140 ...  .. annotations: 1
processing orphanet number: 1293 ...  .. annotations: 3
processing orphanet number: 3471 ...  .. annotations: 5
adding alternatives:[Young syndrome, Azoospermia - sinopulmonary infections, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3471]
processing orphanet number: 1292 ...  .. annotations: 35
adding alternatives:[Brachymorphism - onychodysplasia - dysphalangism, BOD syndrome, Senior syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1292]
processing orphanet number: 319600 ...  .. annotations: 4
NO OMIMENTRY FOR OMIM-ID 614893 creating NEW one
processing orphanet number: 2139 ...  .. annotations: 11
processing orphanet number: 861 ...  .. annotations: 64
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2138 ...  .. annotations: 14
adding alternatives:[46,XX ovotesticular disorder of sex development, 46,XX ovotesticular DSD, True hermaphroditism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2138, 46,XX testicular disorder of sex development, 46,XX testicular DSD, De la Chapelle syndrome, XX, male syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=393]
  ... no hpo-term mapping for orphanet annotation: 52000
processing orphanet number: 3469 ...  .. annotations: 13
adding alternatives:[XK aprosencephaly, Atelencephaly, Garcia-Lurie syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3469]
processing orphanet number: 2136 ...  .. annotations: 52
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2135 ...  .. annotations: 37
adding alternatives:[Hennekam-Beemer syndrome, Mastocytosis - short stature - hearing loss, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2135]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 3466 ...  .. annotations: 17
adding alternatives:[WT limb-blood syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3466]
processing orphanet number: 3465 ...  .. annotations: 9
adding alternatives:[Worster-Drought syndrome, Congenital suprabulbar paresis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3465]
processing orphanet number: 867 ...  .. annotations: 6
processing orphanet number: 868 ...  .. annotations: 9
adding alternatives:[Triose phosphate-isomerase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=868]
processing orphanet number: 869 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 50943 ...  .. annotations: 4
adding alternatives:[Keratolytic winter erythema, Erythrokeratolysis hiemalis, Oudtshoorn disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50943]
processing orphanet number: 50942 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 50945 ...  .. annotations: 30
adding alternatives:[Blomstrand lethal chondrodysplasia, BLC, BOCD, Blomstrand chondrodysplasia, Blomstrand osteochondrodysplasia, Chondrodysplasia, Blomstrand type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50945]
processing orphanet number: 178377 ...  .. annotations: 17
processing orphanet number: 50944 ...  .. annotations: 11
adding alternatives:[Schöpf-Schulz-Passarge syndrome, Eccrine tumors-ectodermal dysplasia, Keratosis palmoplantaris - cystic eyelids - hypodontia - hypotrichosis, Palmoplantar hyperkeratosis - cystic eyelids - hypodontia - hypotrichosis, Palmoplantar keratoderma - cystic eyelids - hypodontia - hypotrichosis, SSPS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=50944]
processing orphanet number: 75325 ...  .. annotations: 5
NO OMIMENTRY FOR OMIM-ID 609993 creating NEW one
processing orphanet number: 2155 ...  .. annotations: 8
adding alternatives:[Hirschsprung disease - deafness - polydactyly, Santos-Mateus-Leal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2155]
processing orphanet number: 3000 ...  .. annotations: 12
adding alternatives:[Familial male-limited precocious puberty, FMPP, Familial gonadotropin-independent male-limited sexual precocity, Male-limited precocious puberty, Testotoxicosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3000]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2153 ...  .. annotations: 21
adding alternatives:[Hirschsprung disease-nail hypoplasia-dysmorphism, Al Gazali-Donnai-Muller syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2153]
processing orphanet number: 2152 ...  .. annotations: 50
adding alternatives:[Mowat-Wilson syndrome, Hirschsprung disease - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2152]
processing orphanet number: 99776 ...  .. annotations: 63
processing orphanet number: 2151 ...  .. annotations: 6
processing orphanet number: 2150 ...  .. annotations: 8
adding alternatives:[Hirschsprung disease - type D brachydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2150]
processing orphanet number: 96263 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 96264 ...  .. annotations: 57
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 870 ...  .. annotations: 48
processing orphanet number: 871 ...  .. annotations: 1
processing orphanet number: 2149 ...  .. annotations: 4
processing orphanet number: 2148 ...  .. annotations: 5
adding alternatives:[Lissencephaly type 1 due to doublecortin gene mutation, X-linked lissencephaly type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2148, Subcortical band heterotopia, Subcortical laminar heterotopia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99796]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 873 ...  .. annotations: 21
adding alternatives:[Desmoid tumor, Aggressive fibromatosis, Desmoid type fibromatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=873]
  ... no hpo-term mapping for orphanet annotation: 45510
processing orphanet number: 2145 ...  .. annotations: 25
processing orphanet number: 88644 ...  .. annotations: 1
adding alternatives:[Autosomal recessive ataxia, Beauce type, ARCA1, Autosomal recessive cerebellar ataxia type 1, SCAR8, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=88644]
processing orphanet number: 88643 ...  .. annotations: 3
processing orphanet number: 101041 ...  .. annotations: 5
adding alternatives:[Congenital fibrinogen deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=335, Familial afibrinogenemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98880, Familial hypofibrinogenemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101041]
processing orphanet number: 163746 ...  .. annotations: 31
adding alternatives:[Neurologic Waardenburg-Shah syndrome, PCWH, Peripheral demyelinating neuropathy - central dysmyelinating leukodystrophy - Waardenburg syndrome - Hirschsprung disease, WS4 plus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163746]
processing orphanet number: 2166 ...  .. annotations: 37
adding alternatives:[Holoprosencephaly - postaxial polydactyly, Pseudo-trisomy 13 syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2166]
processing orphanet number: 206583 ...  .. annotations: 20
adding alternatives:[Glycogen storage disease due to glycogen branching enzyme deficiency, Amylopectinosis, Andersen disease, GSD due to glycogen branching enzyme deficiency, GSD type 4, Glycogen storage disease type 4, Glycogenosis due to glycogen branching enzyme deficiency, Glycogenosis type 4, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=367, Adult polyglucosan body disease, APBD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=206583]
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 2165 ...  .. annotations: 18
processing orphanet number: 3011 ...  .. annotations: 4
adding alternatives:[Spastic tetraplegia - retinitis pigmentosa - intellectual disability, Spastic quadriplegia - retinitis pigmentosa - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3011]
processing orphanet number: 2163 ...  .. annotations: 23
adding alternatives:[Holoprosencephaly - craniosynostosis, Camero-Lituania-Cohen syndrome, Genoa syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2163]
processing orphanet number: 3010 ...  .. annotations: 21
adding alternatives:[Qazi-Markouizos syndrome, Dysharmonic skeletal maturation - muscular fiber disproportion, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3010]
processing orphanet number: 2162 ...  .. annotations: 90
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 96253 ...  .. annotations: 40
adding alternatives:[Cushing disease, Corticotroph pituitary adenoma, Pituitary corticotroph micro-adenoma, Pituitary dependent Cushing syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=96253]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 881 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 52420
processing orphanet number: 276422 ...  .. annotations: 21
processing orphanet number: 882 ...  .. annotations: 6
adding alternatives:[Tyrosinemia type 1, FAH deficiency, Fumarylacetoacetase deficiency, Fumarylacetoacetate hydrolase deficiency, Hepatorenal tyrosinemia, Tyrosinemia type I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=882]
processing orphanet number: 88639 ...  .. annotations: 1
adding alternatives:[Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency, HIBCH deficiency, Methacrylic aciduria, Valine metabolic defect, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=88639]
processing orphanet number: 884 ...  .. annotations: 28
adding alternatives:[Tetrasomy 12p, Isochromosome 12p mosaicism, Isochromosome 12p syndrome, Pallister-Killian syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=884]
processing orphanet number: 3006 ...  .. annotations: 12
adding alternatives:[Pyridoxine-dependent epilepsy, Antiquitin deficiency, Vitamin B6-dependent seizures, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3006]
processing orphanet number: 400 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 2158 ...  .. annotations: 12
adding alternatives:[Histidinuria - renal tubular defect, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2158]
processing orphanet number: 3005 ...  .. annotations: 16
adding alternatives:[Pyle disease, Metaphyseal dysplasia, Pyle type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3005]
processing orphanet number: 88637 ...  .. annotations: 3
processing orphanet number: 886 ...  .. annotations: 32
processing orphanet number: 3004 ...  .. annotations: 7
processing orphanet number: 887 ...  .. annotations: 42
adding alternatives:[VACTERL/VATER association, VACTERL association, VATER association, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=887]
processing orphanet number: 2156 ...  .. annotations: 27
adding alternatives:[Hirsutism-skeletal dysplasia-intellectual disability syndrome, Wiedemann-Oldigs-Oppermann syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2156]
processing orphanet number: 3003 ...  .. annotations: 17
adding alternatives:[Pyknoachondrogenesis, Camera syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3003]
processing orphanet number: 88635 ...  .. annotations: 1
adding alternatives:[Myopathy due to calsequestrin and SERCA1 protein overload, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=88635]
processing orphanet number: 888 ...  .. annotations: 7
processing orphanet number: 889 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 408 ...  .. annotations: 18
adding alternatives:[Isolated glycerol kinase deficiency, Hyperglycerolemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=408]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 409 ...  .. annotations: 7
adding alternatives:[Hyperkeratosis lenticularis perstans, Flegel disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=409]
processing orphanet number: 99797 ...  .. annotations: 2
adding alternatives:[Anodontia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99797]
processing orphanet number: 2176 ...  .. annotations: 29
NO OMIMENTRY FOR OMIM-ID 236490 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3023 ...  .. annotations: 7
adding alternatives:[Rasmussen-Johnsen-Thomsen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3023]
processing orphanet number: 3021 ...  .. annotations: 17
adding alternatives:[RAPADILINO syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3021]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 99798 ...  .. annotations: 8
processing orphanet number: 2172 ...  .. annotations: 13
adding alternatives:[Microcephaly - glomerulonephritis - marfanoid habitus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2172]
processing orphanet number: 892 ...  .. annotations: 45
adding alternatives:[Von Hippel-Lindau disease, Familial cerebelloretinal angiomatosis, Lindau disease, VHL, Von Hippel-Lindau syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=892]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 39580
processing orphanet number: 893 ...  .. annotations: 18
processing orphanet number: 3019 ...  .. annotations: 20
adding alternatives:[Ramon syndrome, Cherubism - gingival fibromatosis - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3019]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 894 ...  .. annotations: 31
adding alternatives:[Waardenburg syndrome type 1, WS1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=894, Waardenburg syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3440]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 3018 ...  .. annotations: 20
adding alternatives:[Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications, Rambaud-Gallian syndrome, Rambaud-Gallian-Touchard syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3018]
processing orphanet number: 895 ...  .. annotations: 13
processing orphanet number: 896 ...  .. annotations: 24
adding alternatives:[Waardenburg syndrome type 3, Klein-Waardenburg syndrome, WS3, Waardenburg syndrome with limb anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=896, Waardenburg syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3440]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2169 ...  .. annotations: 9
adding alternatives:[Methylcobalamin deficiency type cblE, Functional methionine synthase deficiency type cblE, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2169, Homocystinuria without methylmalonic aciduria, Functional methionine synthase deficiency, Methylcobalamin deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=622]
processing orphanet number: 3016 ...  .. annotations: 7
adding alternatives:[Radius absent - anogenital anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3016]
processing orphanet number: 897 ...  .. annotations: 22
processing orphanet number: 3015 ...  .. annotations: 18
adding alternatives:[Radio-renal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3015]
processing orphanet number: 33110 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2167 ...  .. annotations: 22
adding alternatives:[Holzgreve-Wagner-Rehder syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2167]
processing orphanet number: 276413 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 33111 ...  .. annotations: 6
processing orphanet number: 899 ...  .. annotations: 36
processing orphanet number: 416 ...  .. annotations: 10
processing orphanet number: 417 ...  .. annotations: 12
adding alternatives:[Neonatal severe primary hyperparathyroidism, NSHPT, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=417]
processing orphanet number: 228384 ...  .. annotations: 25
adding alternatives:[5q14.3 microdeletion syndrome, Del(5)(q14.3), Monosomy 5q14.3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228384]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 418 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 419 ...  .. annotations: 5
adding alternatives:[Hyperprolinemia type 1, Proline oxidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=419]
processing orphanet number: 2180 ...  .. annotations: 30
adding alternatives:[Hydrocephalus - costovertebral dysplasia - Sprengel anomaly, Ferlini-Ragno-Calzolari syndrome, Waaler-Aarskog syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2180]
processing orphanet number: 90970 ...  .. annotations: 21
processing orphanet number: 3035 ...  .. annotations: 15
adding alternatives:[Growth delay - hydrocephaly - lung hypoplasia, Game-Friedman-Paradice syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3035]
processing orphanet number: 3034 ...  .. annotations: 8
adding alternatives:[Delayed membranous cranial ossification, Gonzales-del Angel syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3034]
processing orphanet number: 2186 ...  .. annotations: 28
processing orphanet number: 3033 ...  .. annotations: 14
adding alternatives:[Renal tubular dysgenesis, Primitive renal tubule syndrome, Renotubular dysgenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3033, Renal tubular dysgenesis of genetic origin, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97369]
processing orphanet number: 94095 ...  .. annotations: 19
adding alternatives:[Spondylocostal dysostosis - anal and genitourinary malformations, Casamassima-Morton-Nance syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=94095]
processing orphanet number: 2185 ...  .. annotations: 2
processing orphanet number: 3032 ...  .. annotations: 9
adding alternatives:[NPHP3-related Meckel-like syndrome, Goldston syndrome, Meckel syndrome type 7, Meckel-like syndrome type 1, Renal-hepatic-pancreatic dysplasia - Dandy-Walker cysts, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3032]
processing orphanet number: 2184 ...  .. annotations: 10
processing orphanet number: 2183 ...  .. annotations: 9
processing orphanet number: 2182 ...  .. annotations: 16
adding alternatives:[Hydrocephalus with stenosis of the aqueduct of Sylvius, Bickers-Adams syndrome, HSAS, X-linked HSAS, X-linked acqueductal stenosis, X-linked hydrocephalus, X-linked hydrocephalus with stenosis of aqueduct of Sylvius, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2182, L1 syndrome, CRASH syndrome, Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome, L1CAM syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=275543]
processing orphanet number: 169079 ...  .. annotations: 13
NO OMIMENTRY FOR OMIM-ID 611291 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2181 ...  .. annotations: 16
adding alternatives:[Hydrocephaly - tall stature - joint laxity, Daish-Hardman-Lamont syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2181]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 220402 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 20160
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 3029 ...  .. annotations: 1
processing orphanet number: 3027 ...  .. annotations: 29
adding alternatives:[Sirenomelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3169, Caudal regression sequence, Caudal dysplasia, Sacral agenesis syndrome, Sacral regression syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3027, Familial caudal dysgenesis, Rudd-Klimek syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1768]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43180
processing orphanet number: 3026 ...  .. annotations: 11
adding alternatives:[Radial ray hypoplasia - choanal atresia, Goldblatt-Viljoen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3026]
processing orphanet number: 425 ...  .. annotations: 10
adding alternatives:[Apolipoprotein A-I deficiency, ApoA-I deficiency, Familial apoA-I deficiency, Familial hypoalphalipoproteinemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=425]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 228371 ...  .. annotations: 19
processing orphanet number: 428 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 429 ...  .. annotations: 21
adding alternatives:[Hypochondroplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=429]
processing orphanet number: 33108 ...  .. annotations: 39
adding alternatives:[Lethal multiple pterygium syndrome, Autosomal recessive lethal multiple pterygium syndrome, LMPS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33108]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 85170 ...  .. annotations: 13
adding alternatives:[Mesomelic dysplasia, Savarirayan type, Mesomelic dysplasia with absent fibulas and triangular tibias, Triangular tibia - fibular aplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85170]
processing orphanet number: 2190 ...  .. annotations: 7
adding alternatives:[Congenital hydronephrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2190]
processing orphanet number: 85172 ...  .. annotations: 12
processing orphanet number: 101075 ...  .. annotations: 21
adding alternatives:[X-linked Charcot-Marie-Tooth disease type 1, CMT1X, CMTX1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101075]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 101076 ...  .. annotations: 21
adding alternatives:[X-linked Charcot-Marie-Tooth disease type 2, CMT2X, CMTX2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101076]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 101077 ...  .. annotations: 18
adding alternatives:[X-linked Charcot-Marie-Tooth disease type 3, CMT3X, CMTX3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101077]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 101078 ...  .. annotations: 21
adding alternatives:[X-linked Charcot-Marie-Tooth disease type 4, CMT4X, CMTX4, Cowchock syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101078]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2199 ...  .. annotations: 8
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2199]
processing orphanet number: 2198 ...  .. annotations: 15
adding alternatives:[Palmoplantar keratoderma-esophageal carcinoma syndrome, Bennion-Patterson syndrome, Howell-Evans syndrome, Keratosis palmoplantaris-esophageal carcinoma syndrome, Palmoplantar hyperkeratosis-esophageal carcinoma syndrome, Tylosis - oesophageal carcinoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2198]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3044 ...  .. annotations: 16
adding alternatives:[Intellectual disability - dysmorphism - hypogonadism - diabetes mellitus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3044]
processing orphanet number: 2196 ...  .. annotations: 11
adding alternatives:[Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement, FHHNC with severe ocular involvement, Hypercalciuria - bilateral macular coloboma, Meier-Blumberg-Imahorn syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2196]
processing orphanet number: 3042 ...  .. annotations: 31
adding alternatives:[Intellectual disability - cataracts - calcified pinnae - myopathy, Primrose syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3042]
processing orphanet number: 3041 ...  .. annotations: 35
adding alternatives:[Intellectual disability - balding - patella luxation - acromicria, Scholte-Begeer-van Essen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3041]
processing orphanet number: 33577 ...  .. annotations: 15
processing orphanet number: 33574 ...  .. annotations: 2
adding alternatives:[Gamma-glutamylcysteine synthetase deficiency, Glutamate-cysteine ligase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33574]
processing orphanet number: 3038 ...  .. annotations: 15
adding alternatives:[Delayed speech - facial asymmetry - strabismus - ear lobe creases, Mehes syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3038]
processing orphanet number: 435 ...  .. annotations: 45
adding alternatives:[Ito hypomelanosis, HI syndrome, Hypomelanosis of Ito, Incontinentia pigmenti type 1, Pigmentary mosaicism, Ito type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=435]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 33572 ...  .. annotations: 1
adding alternatives:[5-oxoprolinase deficiency, Oxoprolinuria due to oxoprolinase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33572]
processing orphanet number: 436 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2189 ...  .. annotations: 23
processing orphanet number: 33573 ...  .. annotations: 1
adding alternatives:[Gamma-glutamyl transpeptidase deficiency, Glutathionuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33573]
processing orphanet number: 437 ...  .. annotations: 12
processing orphanet number: 85174 ...  .. annotations: 7
adding alternatives:[Pseudodiastrophic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85174]
processing orphanet number: 85173 ...  .. annotations: 13
adding alternatives:[IMAGe syndrome, Intrauterine growth retardation - metaphyseal dysplasia - adrenal hypoplasia congenita - genital anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85173]
processing orphanet number: 231568 ...  .. annotations: 16
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231568]
processing orphanet number: 85175 ...  .. annotations: 4
processing orphanet number: 163703 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 3057 ...  .. annotations: 3
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3057]
processing orphanet number: 75378 ...  .. annotations: 3
processing orphanet number: 3055 ...  .. annotations: 18
processing orphanet number: 3052 ...  .. annotations: 37
adding alternatives:[X-linked intellectual disability - seizures - psoriasis, Tranebjaerg-Svejgaard syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3052]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 20340
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 75374 ...  .. annotations: 2
NO OMIMENTRY FOR OMIM-ID 608415 creating NEW one
processing orphanet number: 3051 ...  .. annotations: 37
adding alternatives:[Intellectual disability - sparse hair - brachydactyly, Nicolaides-Baraitser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3051]
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 75373 ...  .. annotations: 4
adding alternatives:[Progressive bifocal chorioretinal atrophy, CRAPB, PBCRA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75373]
processing orphanet number: 3050 ...  .. annotations: 21
processing orphanet number: 440 ...  .. annotations: 1
processing orphanet number: 442 ...  .. annotations: 45
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 444 ...  .. annotations: 6
processing orphanet number: 228396 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 446 ...  .. annotations: 13
adding alternatives:[Neonatal hemochromatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=446]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 228399 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3047 ...  .. annotations: 31
adding alternatives:[Blepharophimosis-intellectual disability syndrome, SBBYS type, Hypothyroidism - dysmorphism - postaxial polydactyly - intellectual disability, SBBYSS, Say-Barber-Biesecker-Young-Simpson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3047]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 85167 ...  .. annotations: 19
adding alternatives:[Spondylometaphyseal dysplasia - cone-rod dystrophy, SMD-CRD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85167]
processing orphanet number: 85166 ...  .. annotations: 24
adding alternatives:[Platyspondylic dysplasia, Torrance type, PLSD-T, Platyspondylic dysplasia, Torrance-Luton type, Platyspondylic lethal skeletal dysplasia, Torrance type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85166]
processing orphanet number: 85169 ...  .. annotations: 4
adding alternatives:[Familial digital arthropathy-brachydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85169]
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 85168 ...  .. annotations: 5
processing orphanet number: 85163 ...  .. annotations: 2
adding alternatives:[Hypomyelination - congenital cataract, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85163]
processing orphanet number: 85162 ...  .. annotations: 1
processing orphanet number: 85165 ...  .. annotations: 7
adding alternatives:[Severe achondroplasia - developmental delay - acanthosis nigricans, SADDAN, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85165]
processing orphanet number: 228390 ...  .. annotations: 29
adding alternatives:[Frontonasal dysplasia with alopecia and genital anomaly, ALX4-related FNDAG, Craniofrontonasal dysplasia with alopecia and hypogonadism, Frontonasal dysplasia with alopecia and genital abnomality, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228390]
processing orphanet number: 85164 ...  .. annotations: 4
adding alternatives:[Camptodactyly - tall stature - scoliosis - hearing loss, CATSHL syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85164]
processing orphanet number: 85194 ...  .. annotations: 30
adding alternatives:[Spondylo-ocular syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85194]
processing orphanet number: 85193 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 3068 ...  .. annotations: 32
adding alternatives:[Intellectual disability - myopathy - short stature - endocrine defect, Chudley-Rozdilsky syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3068]
processing orphanet number: 3067 ...  .. annotations: 11
processing orphanet number: 75389 ...  .. annotations: 21
processing orphanet number: 452 ...  .. annotations: 21
adding alternatives:[X-linked lissencephaly with abnormal genitalia, X-linked lissencephaly - agenesis of the corpus callosum - genital anomalies, X-linked lissencephaly with ambiguous genitalia, XLAG syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=452]
processing orphanet number: 454 ...  .. annotations: 15
processing orphanet number: 455 ...  .. annotations: 8
adding alternatives:[Superficial epidermolytic ichthyosis, Ichthyosis bullosa of Siemens, SEI, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=455]
processing orphanet number: 457 ...  .. annotations: 20
adding alternatives:[Harlequin ichthyosis, HI, Ichthyosis congenita, harlequin type, Ichthyosis fetalis, Harlequin type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=457]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 85199 ...  .. annotations: 20
adding alternatives:[Craniosynostosis - anal anomalies - porokeratosis, CAP syndrome, CDAGS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85199]
processing orphanet number: 35737 ...  .. annotations: 8
adding alternatives:[Morning glory syndrome, Ectasic coloboma, Volubilis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35737]
processing orphanet number: 85198 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 85197 ...  .. annotations: 4
adding alternatives:[Genochondromatosis type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85197, Genochondromatosis type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93398]
processing orphanet number: 3071 ...  .. annotations: 46
adding alternatives:[Costello syndrome, FCS syndrome, Faciocutaneoskeletal syndrome, Intellectual disability - nasal papillomata, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3071]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 55540
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 3079 ...  .. annotations: 30
adding alternatives:[Intellectual disability, Buenos-Aires type, Mutchinick syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3079]
processing orphanet number: 3078 ...  .. annotations: 10
adding alternatives:[Severe X-linked intellectual disability, Gustavson type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3078]
processing orphanet number: 3077 ...  .. annotations: 13
adding alternatives:[X-linked intellectual disability - psychosis - macroorchidism, Lindsay-Burn syndrome, PPM-X, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3077]
processing orphanet number: 3074 ...  .. annotations: 10
processing orphanet number: 461 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 462 ...  .. annotations: 5
processing orphanet number: 75392 ...  .. annotations: 10
adding alternatives:[Ehlers-Danlos syndrome, periodontitis type, EDS VIII, Ehlers-Danlos syndrome type 8, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75392]
processing orphanet number: 464 ...  .. annotations: 64
adding alternatives:[Incontinentia pigmenti, Bloch-Siemens syndrome, Bloch-Sulzberger syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=464]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 3082 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 98848 ...  .. annotations: 13
processing orphanet number: 3080 ...  .. annotations: 27
adding alternatives:[Intellectual disability, Wolff type, Wolff-Zimmermann syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3080]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 98849 ...  .. annotations: 4
processing orphanet number: 48104 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 3088 ...  .. annotations: 15
adding alternatives:[Revesz syndrome, Dyskeratosis congenita with bilateral exudative retinopathy, Retinopathy-anemia-central nervous system anomalies syndrome, Revesz-DeBuse syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3088]
processing orphanet number: 29822 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 3087 ...  .. annotations: 20
adding alternatives:[Retinohepatoendocrinologic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3087]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 3086 ...  .. annotations: 4
adding alternatives:[MRCS syndrome, Microcornea - rod-cone dystrophy - cataract - posterior staphyloma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=263347, Autosomal dominant vitreoretinochoroidopathy, ADVIRC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3086]
processing orphanet number: 3085 ...  .. annotations: 28
adding alternatives:[Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3085]
processing orphanet number: 474 ...  .. annotations: 25
processing orphanet number: 475 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 26790 ...  .. annotations: 19
processing orphanet number: 477 ...  .. annotations: 49
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 478 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 40540
processing orphanet number: 3090 ...  .. annotations: 5
processing orphanet number: 3099 ...  .. annotations: 36
adding alternatives:[Rheumatic fever, Acute rheumatic fever, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3099]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 3098 ...  .. annotations: 27
adding alternatives:[Rhizomelic syndrome, Urbach type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3098]
processing orphanet number: 480 ...  .. annotations: 14
adding alternatives:[Kearns-Sayre syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=480]
processing orphanet number: 3097 ...  .. annotations: 22
NO OMIMENTRY FOR OMIM-ID 608978 creating NEW one
processing orphanet number: 481 ...  .. annotations: 12
adding alternatives:[Kennedy disease, SBMA, SMAX1-related spinobulbar muscular atrophy, X-linked BSMA, X-linked bulbospinal amyotrophy, X-linked bulbospinal muscular atrophy, X-linked spinal and bulbar muscular atrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=481]
processing orphanet number: 3095 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 484 ...  .. annotations: 25
processing orphanet number: 485 ...  .. annotations: 38
adding alternatives:[Kniest dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=485]
processing orphanet number: 487 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 220497 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 492 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 493 ...  .. annotations: 9
processing orphanet number: 494 ...  .. annotations: 17
adding alternatives:[Keratoderma hereditarium mutilans, Mutilating keratoderma of Vohwinkel, Mutilating keratoderma plus deafness, PPK mutilans and deafness, Vohwinkel syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=494]
  ... no hpo-term mapping for orphanet annotation: 46000
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 495 ...  .. annotations: 10
adding alternatives:[Transgrediens et progrediens palmoplantar keratoderma, Greither disease, Keratosis extremitatum hereditaria progrediens, Keratosis palmoplantaris transgrediens et progrediens, Progressive diffuse PPK, Progressive diffuse palmoplantar keratoderma, Transgrediens et progrediens PPK, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=495, Erythrokeratodermia variabilis, EKV, Erythrokeratodermia variabilis, Mendes da Costa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=317]
processing orphanet number: 498 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 23490
processing orphanet number: 363705 ...  .. annotations: 28
adding alternatives:[Craniofaciofrontodigital syndrome, Cantu craniofaciofrontodigital syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=363705]
processing orphanet number: 499 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 23490
processing orphanet number: 69063 ...  .. annotations: 1
processing orphanet number: 69061 ...  .. annotations: 2
adding alternatives:[Familial idiopathic steroid-resistant nephrotic syndrome, Familial idiopathic nephrotic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=656, Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69061]
processing orphanet number: 157801 ...  .. annotations: 12
adding alternatives:[Mesoaxial synostotic syndactyly with phalangeal reduction, MSSD, Syndactyly type 9, Syndactyly, Malik-Percin type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157801]
processing orphanet number: 98850 ...  .. annotations: 46
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 93160 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 220489 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 220493 ...  .. annotations: 38
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 33067 ...  .. annotations: 20
adding alternatives:[Metaphyseal chondrodysplasia, Jansen type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33067]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 69078 ...  .. annotations: 6
adding alternatives:[Liposarcoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69078, Myxoid/round cell liposarcoma, MRCLS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99967]
processing orphanet number: 69077 ...  .. annotations: 24
processing orphanet number: 99735 ...  .. annotations: 26
adding alternatives:[Potassium-aggravated myotonia, K+-aggravated myotonia, K-aggravated myotonia, PAM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=612, Myotonia fluctuans, Exercise-induced delayed-onset myotonia, Fluctuating myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99734, Myotonia permanens, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99735, Acetazolamide-responsive myotonia, ACZ-responsive congenital myotonia, ACZ-responsive myotonia, Acetazolamide-responsive congenital myotonia, Myotonia - painful contractions, Painful congenital myotonia, Painful myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99736]
processing orphanet number: 99734 ...  .. annotations: 19
adding alternatives:[Potassium-aggravated myotonia, K+-aggravated myotonia, K-aggravated myotonia, PAM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=612, Myotonia fluctuans, Exercise-induced delayed-onset myotonia, Fluctuating myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99734, Myotonia permanens, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99735, Acetazolamide-responsive myotonia, ACZ-responsive congenital myotonia, ACZ-responsive myotonia, Acetazolamide-responsive congenital myotonia, Myotonia - painful contractions, Painful congenital myotonia, Painful myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99736]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 99736 ...  .. annotations: 13
adding alternatives:[Potassium-aggravated myotonia, K+-aggravated myotonia, K-aggravated myotonia, PAM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=612, Myotonia fluctuans, Exercise-induced delayed-onset myotonia, Fluctuating myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99734, Myotonia permanens, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99735, Acetazolamide-responsive myotonia, ACZ-responsive congenital myotonia, ACZ-responsive myotonia, Acetazolamide-responsive congenital myotonia, Myotonia - painful contractions, Painful congenital myotonia, Painful myotonia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99736]
processing orphanet number: 98880 ...  .. annotations: 8
adding alternatives:[Congenital fibrinogen deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=335, Familial afibrinogenemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98880, Familial hypofibrinogenemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101041]
processing orphanet number: 98881 ...  .. annotations: 6
NO OMIMENTRY FOR OMIM-ID 616004 creating NEW one
processing orphanet number: 89937 ...  .. annotations: 16
adding alternatives:[Autosomal dominant hypophosphatemic rickets, ADHR, Autosomal dominant hypophosphatemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89937]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 89936 ...  .. annotations: 15
adding alternatives:[X-linked hypophosphatemia, X-linked hypophosphatemic rickets, XLH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89936]
processing orphanet number: 139578 ...  .. annotations: 13
adding alternatives:[Hereditary sensory and autonomic neuropathy with spastic paraplegia, HSAN with spastic paraplegia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139578]
processing orphanet number: 231169 ...  .. annotations: 18
processing orphanet number: 69087 ...  .. annotations: 6
adding alternatives:[Naegeli-Franceschetti-Jadassohn syndrome, NFJ syndrome, Naegeli syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69087]
processing orphanet number: 231154 ...  .. annotations: 10
NO OMIMENTRY FOR OMIM-ID 609889 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 1707 ...  .. annotations: 31
processing orphanet number: 86893 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1706 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1705 ...  .. annotations: 10
processing orphanet number: 1703 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1702 ...  .. annotations: 27
processing orphanet number: 46348 ...  .. annotations: 2
adding alternatives:[Paroxysmal extreme pain disorder, Familial rectal pain, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46348]
processing orphanet number: 98428 ...  .. annotations: 16
processing orphanet number: 94064 ...  .. annotations: 4
adding alternatives:[Deafness-infertility syndrome, DIS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=94064]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 94063 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 163693 ...  .. annotations: 18
adding alternatives:[2p21 microdeletion syndrome, 2p21 deletion syndrome, Del(2)(p21), Monosomy 2p21, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163693, Hypotonia-cystinuria syndrome, HCS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163690, Atypical hypotonia - cystinuria syndrome, Atypical HCS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238523]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 94068 ...  .. annotations: 26
adding alternatives:[Spondyloepiphyseal dysplasia congenita, Congenital spondyloepiphyseal dysplasia, SEDC, Spranger-Wiedemann disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=94068]
processing orphanet number: 94066 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 94065 ...  .. annotations: 55
adding alternatives:[15q24 microdeletion syndrome, Del(15)(q24), Monosomy 15q24, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=94065]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 85112 ...  .. annotations: 1
NO OMIMENTRY FOR OMIM-ID 610644 creating NEW one
processing orphanet number: 88621 ...  .. annotations: 2
NO OMIMENTRY FOR OMIM-ID 608649 creating NEW one
processing orphanet number: 1716 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 1713 ...  .. annotations: 30
adding alternatives:[17p11.2 microduplication syndrome, Potocki-Lupski syndrome, Trisomy 17p11.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1713]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 231183 ...  .. annotations: 15
processing orphanet number: 99745 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99748 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99742 ...  .. annotations: 25
adding alternatives:[Amish lethal microcephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99742]
  ... no hpo-term mapping for orphanet annotation: 49020
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 163690 ...  .. annotations: 14
adding alternatives:[2p21 microdeletion syndrome, 2p21 deletion syndrome, Del(2)(p21), Monosomy 2p21, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163693, Hypotonia-cystinuria syndrome, HCS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163690, Atypical hypotonia - cystinuria syndrome, Atypical HCS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238523]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 100924 ...  .. annotations: 13
adding alternatives:[Porphyria due to ALA dehydratase deficiency, ALAD porphyria, Porphyria due to ALAD deficiency, Porphyria due to delta-aminolevulinate dehydratase deficiency, Porphyria of Doss, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100924]
processing orphanet number: 35688 ...  .. annotations: 24
adding alternatives:[Léri-Weill dyschondrosteosis, Léri-Weill syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=240, Madelung deformity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=35688]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 35687 ...  .. annotations: 43
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 231178 ...  .. annotations: 21
processing orphanet number: 1727 ...  .. annotations: 40
adding alternatives:[22q11.2 microduplication syndrome, Dup(22)(q11), Duplication 22q11.2, Trisomy 22q11.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1727]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 90045 ...  .. annotations: 27
adding alternatives:[Hereditary folate malabsorption, Congenital folate malabsorption, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90045]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 91378 ...  .. annotations: 7
processing orphanet number: 319251 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90042 ...  .. annotations: 15
adding alternatives:[Primary familial polycythemia, Congenital erythrocytosis due to erythropoietin receptor mutation, Congenital polycythemia due to erythropoietin receptor mutation, Familial erythrocytosis, PFCP, Primary congenital erythrocytosis, Primary familial and congenital polycythemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90042]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 79254 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1738 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 100976 ...  .. annotations: 2
adding alternatives:[Lamellar ichthyosis, Classic lamellar ichthyosis, Congenital lamellar ichthyosis, LI, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=313, Self-healing collodion baby, SHCB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=281122, Bathing suit ichthyosis, BSI, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100976]
processing orphanet number: 90033 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90035 ...  .. annotations: 9
processing orphanet number: 90037 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90036 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 95720 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79241 ...  .. annotations: 22
adding alternatives:[Biotinidase deficiency, BTD deficiency, Juvenile-onset multiple carboxylase deficiency, Late-onset multiple carboxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79241]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79242 ...  .. annotations: 17
adding alternatives:[Holocarboxylase synthetase deficiency, Early-onset multiple carboxylase deficiency, Neonatal multiple carboxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79242]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1745 ...  .. annotations: 31
processing orphanet number: 1742 ...  .. annotations: 17
processing orphanet number: 95716 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 95717 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 95719 ...  .. annotations: 13
adding alternatives:[Athyreosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95713, Thyroid ectopia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95712, Thyroid hemiagenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95719, Thyroid hypoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95720]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 199251 ...  .. annotations: 7
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 79273 ...  .. annotations: 15
adding alternatives:[Hereditary coproporphyria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79273]
processing orphanet number: 79276 ...  .. annotations: 27
adding alternatives:[Acute intermittent porphyria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79276]
processing orphanet number: 171719 ...  .. annotations: 10
adding alternatives:[Cutis laxa-Marfanoid syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=171719]
processing orphanet number: 1756 ...  .. annotations: 15
adding alternatives:[Caudal duplication, Dipygus, Split notochord syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1756]
processing orphanet number: 79278 ...  .. annotations: 9
processing orphanet number: 79277 ...  .. annotations: 14
adding alternatives:[Congenital erythropoietic porphyria, CEP, Günther disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79277]
processing orphanet number: 2601 ...  .. annotations: 6
processing orphanet number: 79279 ...  .. annotations: 28
adding alternatives:[Alpha-N-acetylgalactosaminidase deficiency, NAGA deficiency, Schindler disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3137, Alpha-N-acetylgalactosaminidase deficiency type 1, NAGA deficiency type 1, Schindler disease type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79279, Alpha-N-acetylgalactosaminidase deficiency type 3, NAGA deficiency type 3, Schindler disease type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79281]
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 1752 ...  .. annotations: 29
processing orphanet number: 168549 ...  .. annotations: 21
adding alternatives:[Axial spondylometaphyseal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168549]
processing orphanet number: 2609 ...  .. annotations: 1
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2609]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 2608 ...  .. annotations: 11
adding alternatives:[N syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2608]
processing orphanet number: 1759 ...  .. annotations: 13
processing orphanet number: 97927 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2604 ...  .. annotations: 26
adding alternatives:[Familial visceral myopathy, Familial hollow visceral myopathy, Hereditary hollow visceral myopathy, Megaduodenum and/or megacystis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2604]
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 1757 ...  .. annotations: 3
processing orphanet number: 91385 ...  .. annotations: 6
adding alternatives:[Acquired angioedema, AAE, Acquired C1 inhibitor deficiency, Acquired angioneurotic edema, Acquired bradykinine-induced angioedema, Acquired non histamine-induced angioedema, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91385, Renin-angiotensin-aldosterone system-blocker-induced angioedema, RAAS-blocker-induced angioedema, RAAS-blocker-induced angioneurotic edema, RAE, Renin-angiotensin-aldosterone system-blocker-induced angioneurotic edema, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100057]
  ... no hpo-term mapping for orphanet annotation: 54840
processing orphanet number: 1770 ...  .. annotations: 27
adding alternatives:[Gonadal dysgenesis, XY type - associated anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1770]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 137817 ...  .. annotations: 16
adding alternatives:[Arachnoiditis, Adhesive arachnoiditis, Chronic arachnoiditis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=137817]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79263 ...  .. annotations: 14
processing orphanet number: 79262 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 79264 ...  .. annotations: 14
processing orphanet number: 2614 ...  .. annotations: 32
adding alternatives:[Nail-patella syndrome, Onychoosteodysplasia, Turner-Kieser syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2614]
processing orphanet number: 1767 ...  .. annotations: 4
adding alternatives:[Familial progressive vestibulocochlear dysfunction, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1767]
processing orphanet number: 1766 ...  .. annotations: 14
processing orphanet number: 2613 ...  .. annotations: 7
adding alternatives:[Nail-patella-like renal disease, Salcedo syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2613]
processing orphanet number: 2612 ...  .. annotations: 31
adding alternatives:[Linear nevus sebaceus syndrome, Nevus sebaceus of Jadassohn, Nevus sebaceus syndrome, Organoid nevus syndrome, Schimmelpenning syndrome, Solomon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2612]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1765 ...  .. annotations: 15
adding alternatives:[Dyschondrosteosis - nephritis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1765]
processing orphanet number: 1764 ...  .. annotations: 37
adding alternatives:[Familial dysautonomia, HSAN3, Hereditary sensory and autonomic neuropathy type 3, Riley-Day syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1764]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2611 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 24920
processing orphanet number: 1762 ...  .. annotations: 15
NO OMIMENTRY FOR OMIM-ID 300815 creating NEW one
processing orphanet number: 2619 ...  .. annotations: 11
adding alternatives:[Brachydactylous dwarfism, Mseleni type, Mseleni joint disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2619]
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 2617 ...  .. annotations: 31
adding alternatives:[Bird headed-dwarfism, Montreal type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2617]
processing orphanet number: 2616 ...  .. annotations: 40
processing orphanet number: 238606 ...  .. annotations: 7
processing orphanet number: 2615 ...  .. annotations: 35
adding alternatives:[Nakajo-Nishimura syndrome, Amyotrophy-fat tissue anomaly syndrome, NNS, Secondary hypertrophic osteoperiostosis with pernio, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2615, JMP syndrome, Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324999, CANDLE syndrome, Chronic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=325004, Proteasome disability syndrome, ALDD syndrome, Autoinflammation-lipodystrophy-dermatoses syndrome, PRAAS, Proteasome-associated autoinflammatory syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324977]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 20380
processing orphanet number: 1768 ...  .. annotations: 15
adding alternatives:[Sirenomelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3169, Caudal regression sequence, Caudal dysplasia, Sacral agenesis syndrome, Sacral regression syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3027, Familial caudal dysgenesis, Rudd-Klimek syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1768]
processing orphanet number: 31709 ...  .. annotations: 8
adding alternatives:[Infantile convulsions and choreoathetosis, ICCA syndrome, Paroxysmal kinesigenic dyskinesia and infantile convulsions, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=31709]
processing orphanet number: 79292 ...  .. annotations: 8
adding alternatives:[LCAT deficiency, Lecithin-cholesterol acyltransferase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=650, Fish-eye disease, FED, Partial LCAT deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79292]
processing orphanet number: 1780 ...  .. annotations: 24
adding alternatives:[Dysmorphism - multiple structural anomalies, Thakker-Donnai syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1780]
processing orphanet number: 189427 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 319218 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 93111 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 39580
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 319213 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 86818 ...  .. annotations: 24
adding alternatives:[Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome, AMME complex, AMME syndrome, ATS-MR, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86818]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 1778 ...  .. annotations: 26
processing orphanet number: 1777 ...  .. annotations: 26
adding alternatives:[Temtamy syndrome, Craniofacial dysmorphism - coloboma - corpus callosum agenesis, Temtamy-Shalash syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1777]
processing orphanet number: 2623 ...  .. annotations: 44
processing orphanet number: 1775 ...  .. annotations: 65
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 26200
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 83317 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 2621 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 1773 ...  .. annotations: 9
processing orphanet number: 1779 ...  .. annotations: 12
processing orphanet number: 189439 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 70482 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 79281 ...  .. annotations: 8
adding alternatives:[Alpha-N-acetylgalactosaminidase deficiency, NAGA deficiency, Schindler disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3137, Alpha-N-acetylgalactosaminidase deficiency type 1, NAGA deficiency type 1, Schindler disease type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79279, Alpha-N-acetylgalactosaminidase deficiency type 3, NAGA deficiency type 3, Schindler disease type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79281]
processing orphanet number: 1791 ...  .. annotations: 35
adding alternatives:[Frontofacionasal dysplasia, Gollop syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1791]
  ... no hpo-term mapping for orphanet annotation: 7550
processing orphanet number: 79280 ...  .. annotations: 14
adding alternatives:[Alpha-N-acetylgalactosaminidase deficiency, NAGA deficiency, Schindler disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3137, Alpha-N-acetylgalactosaminidase deficiency type 2, Adult-onset Alpha-N-acetylgalactosaminidase deficiency, Kanzaki disease, NAGA deficiency type 2, Schindler disease type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79280]
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 1790 ...  .. annotations: 28
adding alternatives:[Hypomandibular faciocranial dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1790]
  ... no hpo-term mapping for orphanet annotation: 26020
processing orphanet number: 300605 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 79283 ...  .. annotations: 12
adding alternatives:[Methylmalonic acidemia with homocystinuria, Combined defect in adenosylcobalamin and methylcobalamin synthesis, Methylmalonic aciduria with homocystinuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=26, Vitamin B12-responsive methylmalonic acidemia, Adenosylcobalamin deficiency, Vitamin B12-responsive methylmalonic aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=28, Homocystinuria without methylmalonic aciduria, Functional methionine synthase deficiency, Methylcobalamin deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=622, Methylcobalamin deficiency type cblDv1, Functional methionine synthase deficiency type cblDv1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=308380, Vitamin B12-responsive methylmalonic acidemia, type cblDv2, Vitamin B12-responsive methylmalonic aciduria, type cblDv2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=308442, Methylmalonic acidemia with homocystinuria, type cblD, CblD defect, Cobalamin D defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD, Methylmalonic aciduria with homocystinuria, type cblD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79283]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79282 ...  .. annotations: 11
adding alternatives:[Methylmalonic acidemia with homocystinuria, Combined defect in adenosylcobalamin and methylcobalamin synthesis, Methylmalonic aciduria with homocystinuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=26, Methylmalonic acidemia with homocystinuria, type cblC, CblC defect, Cobalamin C defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC, Methylmalonic aciduria with homocystinuria, type cblC, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79282]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79284 ...  .. annotations: 12
adding alternatives:[Methylmalonic acidemia with homocystinuria, Combined defect in adenosylcobalamin and methylcobalamin synthesis, Methylmalonic aciduria with homocystinuria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=26, Methylmalonic acidemia with homocystinuria type cblF, CblF defect, Cobalamin F defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF, Lysosomal membrane cobalamin transporter deficiency, Methylmalonic aciduria with homocystinuria, type cblF, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79284]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1305 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 2636 ...  .. annotations: 49
processing orphanet number: 2635 ...  .. annotations: 26
adding alternatives:[Metatropic dysplasia, Metatropic dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2635]
processing orphanet number: 1788 ...  .. annotations: 21
adding alternatives:[Acrofacial dysostosis, Rodríguez type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1788]
processing orphanet number: 2634 ...  .. annotations: 13
adding alternatives:[Mesomelic dwarfism, Reinhardt-Pfeiffer type, Reinhardt-Pfeiffer mesomelic dysplasia, Reinhardt-Pfeiffer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2634]
processing orphanet number: 1787 ...  .. annotations: 28
adding alternatives:[Acrofacial dysostosis, Palagonia type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1787]
processing orphanet number: 1786 ...  .. annotations: 35
NO OMIMENTRY FOR OMIM-ID 101805 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2633 ...  .. annotations: 26
adding alternatives:[Mesomelic dwarfism, Nievergelt type, Nievergelt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2633]
processing orphanet number: 86814 ...  .. annotations: 8
processing orphanet number: 2632 ...  .. annotations: 13
adding alternatives:[Langer mesomelic dysplasia, Mesomelic dwarfism, Langer type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2632]
processing orphanet number: 1300 ...  .. annotations: 26
adding alternatives:[Autosomal dominant popliteal pterygium syndrome, Facio-genito-popliteal syndrome, Popliteal web syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1300]
processing orphanet number: 1784 ...  .. annotations: 27
adding alternatives:[Acro-fronto-facio-nasal dysostosis, Richieri-Costa-Colletto syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1784]
processing orphanet number: 2631 ...  .. annotations: 21
adding alternatives:[Mesomelic dwarfism - cleft palate - camptodactyly, Reardon-Hall-Slaney syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2631]
processing orphanet number: 1782 ...  .. annotations: 21
adding alternatives:[Dysosteosclerosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1782]
processing orphanet number: 1309 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1308 ...  .. annotations: 54
adding alternatives:[C syndrome, OTCS, Opitz C trigonocephaly, Opitz trigonocephaly C syndrome, Opitz trigonocephaly syndrome, Trigonocephaly C syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1308]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 2639 ...  .. annotations: 15
adding alternatives:[Fibular aplasia - complex brachydactyly, Du Pan syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2639]
processing orphanet number: 1307 ...  .. annotations: 30
adding alternatives:[Distal limb deficiencies - micrognathia syndrome, 10q24 microduplication syndrome, Buttiens-Fryns syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1307, Split hand-split foot malformation, Ectrodactyly, Lobster-claw deformity, SHFM, Split hand foot malformation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2440]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 1306 ...  .. annotations: 33
adding alternatives:[Isolated osteopoikilosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166119, Buschke-Ollendorff syndrome, Disseminated dermatofibrosis with osteopoikilosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1306]
processing orphanet number: 2637 ...  .. annotations: 50
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2637]
processing orphanet number: 69028 ...  .. annotations: 10
processing orphanet number: 157850 ...  .. annotations: 29
adding alternatives:[Pantothenate kinase-associated neurodegeneration, Hallervorden-Spatz syndrome, NBIA1, Neurodegeneration with brain iron accumulation type 1, PKAN, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157850]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2650 ...  .. annotations: 11
adding alternatives:[Dwarfism-intellectual disability-eye abnormality syndrome, Mollica-Pavone-Antener syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2650]
processing orphanet number: 1799 ...  .. annotations: 1
adding alternatives:[Familial developmental dysphasia, Billard-Toutain-Maheut syndrome, FOXP2-associated dysphasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1799]
processing orphanet number: 2646 ...  .. annotations: 25
adding alternatives:[Parastremmatic dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2646]
processing orphanet number: 168984 ...  .. annotations: 10
NO OMIMENTRY FOR OMIM-ID 613089 creating NEW one
processing orphanet number: 1314 ...  .. annotations: 9
processing orphanet number: 1798 ...  .. annotations: 40
adding alternatives:[Dysostosis, Stanescu type, Autosomal dominant osteosclerosis, Stanescu type, Craniofacial dysostosis - diaphyseal hyperplasia, Stanescu osteosclerosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1798]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 2645 ...  .. annotations: 20
adding alternatives:[Osteoglophonic dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2645]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1313 ...  .. annotations: 5
adding alternatives:[Infantile choroidocerebral calcification syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1313]
processing orphanet number: 1797 ...  .. annotations: 22
adding alternatives:[Autosomal dominant spondylocostal dysostosis, Autosomal dominant spondylocostal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1797]
processing orphanet number: 2643 ...  .. annotations: 19
adding alternatives:[Microcephalic primordial dwarfism, Toriello type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2643]
processing orphanet number: 1795 ...  .. annotations: 7
adding alternatives:[Peripheral dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1795]
processing orphanet number: 1310 ...  .. annotations: 15
adding alternatives:[Caffey disease, Infantile cortical hyperostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1310]
  ... no hpo-term mapping for orphanet annotation: 43430
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 1794 ...  .. annotations: 21
processing orphanet number: 82004 ...  .. annotations: 17
NO OMIMENTRY FOR OMIM-ID 300537 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 178303 ...  .. annotations: 33
adding alternatives:[8q22.1 microdeletion syndrome, Monosomy 8q22.1, Nablus mask-like facial syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178303]
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 1319 ...  .. annotations: 10
adding alternatives:[Camptobrachydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1319]
processing orphanet number: 1318 ...  .. annotations: 30
adding alternatives:[Campomelia, Cumming type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1318]
  ... no hpo-term mapping for orphanet annotation: 26460
processing orphanet number: 2649 ...  .. annotations: 13
adding alternatives:[Short stature - intellectual disability - eye anomalies - cleft lip/palate, Richieri Costa-Guion Almeida syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2649]
processing orphanet number: 157846 ...  .. annotations: 17
adding alternatives:[Neuroferritinopathy, Adult basal ganglia disease, Ferritin-related neurodegeneration, Hereditary ferritinopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157846]
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 1327 ...  .. annotations: 46
adding alternatives:[Camptodactyly syndrome, Guadalajara type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1327]
processing orphanet number: 2658 ...  .. annotations: 44
adding alternatives:[Lenz-Majewski hyperostotic dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2658]
processing orphanet number: 1326 ...  .. annotations: 12
adding alternatives:[Camptodactyly syndrome, Guadalajara type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1326]
processing orphanet number: 1325 ...  .. annotations: 4
processing orphanet number: 2655 ...  .. annotations: 42
processing orphanet number: 1323 ...  .. annotations: 23
NO OMIMENTRY FOR OMIM-ID 602612 creating NEW one
processing orphanet number: 2653 ...  .. annotations: 16
processing orphanet number: 1321 ...  .. annotations: 10
adding alternatives:[Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia, Goodman camptodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1321]
processing orphanet number: 900 ...  .. annotations: 66
adding alternatives:[Granulomatosis with polyangiitis, GPA, Wegener granulomatosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=900]
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 901 ...  .. annotations: 10
processing orphanet number: 902 ...  .. annotations: 56
adding alternatives:[Werner syndrome, Adult progeria, WS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=902]
  ... no hpo-term mapping for orphanet annotation: 35390
  ... no hpo-term mapping for orphanet annotation: 50070
processing orphanet number: 903 ...  .. annotations: 6
processing orphanet number: 904 ...  .. annotations: 180
adding alternatives:[Williams syndrome, Deletion 7q11.23, Monosomy 7q11.23, Williams-Beuren syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=904]
  ... no hpo-term mapping for orphanet annotation: 43500
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 38160
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 1329 ...  .. annotations: 1
processing orphanet number: 906 ...  .. annotations: 50
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1328 ...  .. annotations: 49
adding alternatives:[Camurati-Engelmann disease, Progressive diaphyseal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1328]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 907 ...  .. annotations: 1
processing orphanet number: 908 ...  .. annotations: 27
adding alternatives:[Fragile X syndrome, FRAXA syndrome, FXS, FraX syndrome, Martin-Bell syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=908]
  ... no hpo-term mapping for orphanet annotation: 52660
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 909 ...  .. annotations: 31
adding alternatives:[Cerebrotendinous xanthomatosis, CTX, Sterol 27-hydroxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=909]
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 158687 ...  .. annotations: 10
adding alternatives:[Lethal acantholytic epidermolysis bullosa, LAEB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=158687]
processing orphanet number: 2672 ...  .. annotations: 9
adding alternatives:[Neuhauser-Eichner-Opitz syndrome, Recurrent encephalophathy of childhood, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2672]
processing orphanet number: 168491 ...  .. annotations: 12
processing orphanet number: 1340 ...  .. annotations: 78
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2671 ...  .. annotations: 47
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 99015 ...  .. annotations: 20
adding alternatives:[Spastic paraplegia type 2, SPG2, Spastic gait type 2, Spastic paraparesis type 2, X-linked spastic paraplegia type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99015]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 2670 ...  .. annotations: 12
adding alternatives:[Pierson syndrome, Microcoria - congenital nephrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2670]
processing orphanet number: 99014 ...  .. annotations: 22
adding alternatives:[X-linked Charcot-Marie-Tooth disease type 5, CMT5X, CMTX5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99014]
  ... no hpo-term mapping for orphanet annotation: 20240
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 1338 ...  .. annotations: 6
adding alternatives:[Heart defect-tongue hamartoma-polysyndactyly syndrome, Ostravik-Lindemann-Solberg syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1338]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 2669 ...  .. annotations: 15
adding alternatives:[Nephrosis - deafness - urinary tract - digital malformations, Braun-Bayer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2669]
processing orphanet number: 79410 ...  .. annotations: 9
adding alternatives:[Pretibial dystrophic epidermolysis bullosa, DEB-Pt, Pretibial DEB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79410]
processing orphanet number: 2668 ...  .. annotations: 9
adding alternatives:[Nephropathy-deafness-hyperparathyroidism syndrome, Edwards-Patton-Dilly syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2668]
processing orphanet number: 1336 ...  .. annotations: 6
NO OMIMENTRY FOR OMIM-ID 144190 creating NEW one
processing orphanet number: 1335 ...  .. annotations: 27
adding alternatives:[Pentalogy of Cantrell, Cantrell deformity, Cantrell syndrome, Thoraco-abdominal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1335]
  ... no hpo-term mapping for orphanet annotation: 55740
processing orphanet number: 2666 ...  .. annotations: 5
processing orphanet number: 228402 ...  .. annotations: 32
adding alternatives:[Autosomal dominant non-syndromic intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178469, 2q23.1 microdeletion syndrome, Del(2)(q23.1), Monosomy 2q23.1, Pseudo-Angelman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228402]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79411 ...  .. annotations: 5
adding alternatives:[Transient bullous dermolysis of the newborn, DEB, bullous dermolysis of the newborn, DEB-BDN, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79411]
processing orphanet number: 1334 ...  .. annotations: 33
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 40540
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2663 ...  .. annotations: 6
adding alternatives:[Nathalie syndrome, Deafness - cataracts - skeletal anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2663]
processing orphanet number: 2662 ...  .. annotations: 27
adding alternatives:[Keipert syndrome, Nasodigitoacoustic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2662]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 910 ...  .. annotations: 60
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 912 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 915 ...  .. annotations: 49
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 916 ...  .. annotations: 13
adding alternatives:[Aase-Smith syndrome, Aase-Smith I syndrome, Hydrocephalus - cleft palate - joint contractures, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=916]
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 90673 ...  .. annotations: 13
adding alternatives:[Hypothyroidism due to TSH receptor mutations, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90673]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 158676 ...  .. annotations: 5
processing orphanet number: 90674 ...  .. annotations: 13
adding alternatives:[Isolated thyroid-stimulating hormone deficiency, Isolated TSH deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90674]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1352 ...  .. annotations: 21
adding alternatives:[Atrioventricular defect - blepharophimosis -radial defects, Houlston-Ironton-Temple syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1352]
processing orphanet number: 229717 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 1350 ...  .. annotations: 24
processing orphanet number: 2680 ...  .. annotations: 6
processing orphanet number: 53271 ...  .. annotations: 18
adding alternatives:[Muenke syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=53271]
processing orphanet number: 99000 ...  .. annotations: 10
processing orphanet number: 168486 ...  .. annotations: 5
adding alternatives:[Congenital neuronal ceroid lipofuscinosis, Congenital NCL, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168486, Late infantile neuronal ceroid lipofuscinosis, Jansky-Bielschowsky disease, LINCL, Late infantile NCL, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168491, CLN10 disease, Cathepsin D deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=228337, Juvenile neuronal ceroid lipofuscinosis, Batten disease, JNCL, Juvenile NCL, Spielmeyer-Vogt disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79264, Adult neuronal ceroid lipofuscinosis, ANCL, Adult NCL, Kufs disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79262]
processing orphanet number: 2679 ...  .. annotations: 20
processing orphanet number: 2678 ...  .. annotations: 3
adding alternatives:[Neurofibromatosis type 6, Familial café-au-lait spots, Multiple café-au-lait spots, Multiple café-au-lait syndrome, NF6, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2678]
processing orphanet number: 79401 ...  .. annotations: 8
adding alternatives:[Epidermolysis bullosa simplex, Ogna type, EBS-O, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79401]
processing orphanet number: 79400 ...  .. annotations: 4
adding alternatives:[Localized epidermolysis bullosa simplex, EBS-loc, Epidermolysis bullosa simplex of palms and soles, Epidermolysis bullosa simplex, Weber-Cockayne type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79400]
processing orphanet number: 1345 ...  .. annotations: 16
processing orphanet number: 2676 ...  .. annotations: 18
processing orphanet number: 79403 ...  .. annotations: 12
adding alternatives:[Junctional epidermolysis bullosa - pyloric atresia, Carmi syndrome, JEB-PA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79403]
processing orphanet number: 79402 ...  .. annotations: 5
adding alternatives:[Localized junctional epidermolysis bullosa, non-Herlitz type, JEB-nH loc, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251393, Junctional epidermolysis bullosa, non-Herlitz type, JEN-nH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89840, Generalized junctional epidermolysis bullosa, non-Herlitz type, GABEB, Generalized atrophic benign epidermolysis bullosa, JEB-nH gen, Junctional epidermolysis bullosa generalisata mitis, Junctional epidermolysis bullosa, Disentis type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79402, Junctional epidermolysis bullosa inversa, EBJ-I, Inverse JEB, JEB-I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79405]
processing orphanet number: 2674 ...  .. annotations: 32
NO OMIMENTRY FOR OMIM-ID 123853 creating NEW one
processing orphanet number: 79405 ...  .. annotations: 3
adding alternatives:[Localized junctional epidermolysis bullosa, non-Herlitz type, JEB-nH loc, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251393, Junctional epidermolysis bullosa, non-Herlitz type, JEN-nH, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=89840, Generalized junctional epidermolysis bullosa, non-Herlitz type, GABEB, Generalized atrophic benign epidermolysis bullosa, JEB-nH gen, Junctional epidermolysis bullosa generalisata mitis, Junctional epidermolysis bullosa, Disentis type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79402, Junctional epidermolysis bullosa inversa, EBJ-I, Inverse JEB, JEB-I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79405]
processing orphanet number: 920 ...  .. annotations: 40
adding alternatives:[Ablepharon macrostomia syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=920]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1342 ...  .. annotations: 6
adding alternatives:[Heart-hand syndrome type 3, Atriodigital dysplasia type 3, Cardiomelic syndrome type 3, Heart-hand syndrome, Spanish type, Heart-limb syndrome type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1342]
processing orphanet number: 2673 ...  .. annotations: 31
adding alternatives:[Neurofaciodigitorenal syndrome, Freire Maia-Pinheiro-Opitz syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2673]
processing orphanet number: 79404 ...  .. annotations: 11
adding alternatives:[Junctional epidermolysis bullosa, Herlitz type, Epidermolysis bullosa letalis, JEB-H, Junctional epidermolysis bullosa generalisata gravis, Junctional epidermolysis bullosa, Herlitz-Pearson type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79404]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 921 ...  .. annotations: 25
adding alternatives:[Abruzzo-Erickson syndrome, CHARGE-like syndrome, Cleft palate-coloboma-deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=921]
processing orphanet number: 158681 ...  .. annotations: 4
NO OMIMENTRY FOR OMIM-ID 609352 creating NEW one
processing orphanet number: 79406 ...  .. annotations: 2
processing orphanet number: 79409 ...  .. annotations: 30
adding alternatives:[Recessive dystrophic epidermolysis bullosa inversa, Dystrophic epidermolysis bullosa inversa, Inverse RDEB, Inverse recessive dystrophic epidermolysis bullosa, RDEB-I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79409, Severe generalized recessive dystrophic epidermolysis bullosa, Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis, Autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type, RDEB generalisata gravis, RDEB, Hallopeau-Siemens type, RDEB-sev gen, Severe generalized RDEB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79408]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 924 ...  .. annotations: 8
processing orphanet number: 79408 ...  .. annotations: 35
adding alternatives:[Recessive dystrophic epidermolysis bullosa inversa, Dystrophic epidermolysis bullosa inversa, Inverse RDEB, Inverse recessive dystrophic epidermolysis bullosa, RDEB-I, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79409, Severe generalized recessive dystrophic epidermolysis bullosa, Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis, Autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type, RDEB generalisata gravis, RDEB, Hallopeau-Siemens type, RDEB-sev gen, Severe generalized RDEB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79408]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 46240
processing orphanet number: 158684 ...  .. annotations: 14
adding alternatives:[Epidermolysis bullosa simplex with pyloric atresia, EBS-PA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=158684]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 65250 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 929 ...  .. annotations: 12
adding alternatives:[Achalasia - microcephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=929]
  ... no hpo-term mapping for orphanet annotation: 26200
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1361 ...  .. annotations: 6
adding alternatives:[Carnosinemia, Carnosinase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1361]
processing orphanet number: 2690 ...  .. annotations: 5
processing orphanet number: 228415 ...  .. annotations: 6
processing orphanet number: 228418 ...  .. annotations: 6
processing orphanet number: 79430 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 79432 ...  .. annotations: 12
adding alternatives:[Oculocutaneous albinism type 2, OCA2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79432]
processing orphanet number: 2206 ...  .. annotations: 5
adding alternatives:[Ankylosing vertebral hyperostosis with tylosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2206]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 1359 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 79431 ...  .. annotations: 16
adding alternatives:[Oculocutaneous albinism type 1, OCA1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352731, Oculocutaneous albinism type 1A, OCA1A, Tyrosinase-negative oculocutaneous albinism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79431]
processing orphanet number: 1358 ...  .. annotations: 35
adding alternatives:[Carey-Fineman-Ziter  syndrome, Myopathy - Moebius - Robin syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1358]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79434 ...  .. annotations: 15
adding alternatives:[Oculocutaneous albinism type 1, OCA1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352731, Temperature-sensitive oculocutaneous albinism type 1, OCA1-TS, TS OCA type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=352737, Oculocutaneous albinism type 1B, OCA1B, Oculocutaneous albinism type Amish, Platinum oculocutaneous albinism, Yellow oculocutaneous albinism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79434]
processing orphanet number: 2204 ...  .. annotations: 14
processing orphanet number: 79433 ...  .. annotations: 7
adding alternatives:[Oculocutaneous albinism type 3, OCA3, Red oculocutaneous albinism, Rufous oculocutaneous albinism, Xanthous oculocutaneous albinism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79433]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1355 ...  .. annotations: 13
adding alternatives:[Heart defect - round face - congenital developmental delay, Sonoda syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1355]
processing orphanet number: 2202 ...  .. annotations: 4
adding alternatives:[Palmoplantar keratoderma-deafness syndrome, PPK-deafness syndrome, Palmoplantar hyperkeratosis-deafness syndrome, Palmoplantar hyperkeratosis-hearing loss syndrome, Palmoplantar keratoderma-hearing loss syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2202]
processing orphanet number: 2686 ...  .. annotations: 15
adding alternatives:[Cyclic neutropenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2686]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 77258 ...  .. annotations: 26
processing orphanet number: 79435 ...  .. annotations: 11
adding alternatives:[Oculocutaneous albinism type 4, OCA4, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79435]
processing orphanet number: 930 ...  .. annotations: 2
adding alternatives:[Idiopathic achalasia, Achalasia cardia, Idiopathic achalasia of esophagus, Primary achalasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=930]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 1354 ...  .. annotations: 15
adding alternatives:[Heart defects - limb shortening, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1354]
processing orphanet number: 2201 ...  .. annotations: 13
adding alternatives:[Palmoplantar keratoderma-spastic paralysis syndrome, Palmoplantar hyperkeratosis-spastic paralysis syndrome, Powell-Venencie-Gordon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2201]
processing orphanet number: 77259 ...  .. annotations: 35
adding alternatives:[Gaucher disease, Acid beta-glucosidase deficiency, Glucocerebrosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355, Gaucher disease type 1, Non-cerebral juvenile Gaucher disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=77259]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 931 ...  .. annotations: 9
adding alternatives:[Acheiropodia, Acheiropody, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=931]
processing orphanet number: 2200 ...  .. annotations: 8
adding alternatives:[Focal palmoplantar and gingival keratoderma, Focal palmoplantar and gingival hyperkeratosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2200]
processing orphanet number: 932 ...  .. annotations: 23
processing orphanet number: 935 ...  .. annotations: 19
adding alternatives:[Short-limb skeletal dysplasia with severe combined immunodeficiency, Achondroplasia-SCID syndrome, Achondroplasia-Swiss type agammaglobulinemia syndrome, Achondroplasia-severe combined immunodeficiency syndrome, Immunodeficiency-short limb dwarfism syndrome, Short limb skeletal dysplasia with SCID, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=935]
processing orphanet number: 939 ...  .. annotations: 16
adding alternatives:[3-hydroxyisobutyric aciduria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=939]
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 91546 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2221 ...  .. annotations: 18
processing orphanet number: 99027 ...  .. annotations: 21
adding alternatives:[Adult-onset autosomal dominant leukodystrophy, ADLD, Adult-onset autosomal dominant demyelinating leukodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99027]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43180
processing orphanet number: 1373 ...  .. annotations: 11
adding alternatives:[Cataract - aberrant oral frenula - growth delay, Wellesley-Carman-French syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1373]
processing orphanet number: 2220 ...  .. annotations: 22
adding alternatives:[Hypertrichosis cubiti - short stature, Hairy elbows, MacDermot-Patton-Williams syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2220]
processing orphanet number: 2218 ...  .. annotations: 6
adding alternatives:[Cervical hypertrichosis - peripheral neuropathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2218]
processing orphanet number: 77243 ...  .. annotations: 8
adding alternatives:[Lipedema, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=77243]
processing orphanet number: 1369 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 2216 ...  .. annotations: 17
processing orphanet number: 1368 ...  .. annotations: 13
adding alternatives:[Cataract - ataxia - deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1368]
processing orphanet number: 2215 ...  .. annotations: 57
adding alternatives:[Malignant hyperthermia - arthrogryposis - torticollis, Froster-Iskenius-Waterson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2215]
  ... no hpo-term mapping for orphanet annotation: 3560
processing orphanet number: 2699 ...  .. annotations: 3
adding alternatives:[Median nodule of the upper lip, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2699]
processing orphanet number: 53296 ...  .. annotations: 12
adding alternatives:[Familial cutaneous collagenoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=53296]
processing orphanet number: 2698 ...  .. annotations: 6
adding alternatives:[Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome, Bart-Pumphrey syndrome, Knuckle pads-leukonychia-sensorineural deafness-palmoplantar keratoderma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2698]
processing orphanet number: 1366 ...  .. annotations: 11
adding alternatives:[Autosomal recessive palmoplantar keratoderma and congenital alopecia, Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia, Cataract - alopecia - sclerodactyly, PPK-CA, Wallis type, Palmoplantar keratoderma and congenital alopecia, Wallis type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1366]
processing orphanet number: 2213 ...  .. annotations: 13
adding alternatives:[Hypertelorism-microtia-facial clefting syndrome, Bixler-Christian-Gorlin syndrome, HMC syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2213]
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 2697 ...  .. annotations: 42
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 228410 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 2211 ...  .. annotations: 25
adding alternatives:[Hypertelorism - hypospadias - polysyndactyly syndrome, Acro-fronto-facio-nasal dysostosis type 2, Acro-fronto-facio-nasal syndrome type 2, Naguib-Richieri-Costa syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2211]
processing orphanet number: 2695 ...  .. annotations: 4
processing orphanet number: 943 ...  .. annotations: 8
adding alternatives:[Malonic aciduria, Malonyl-CoA decarboxylase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=943]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 945 ...  .. annotations: 15
processing orphanet number: 946 ...  .. annotations: 15
processing orphanet number: 949 ...  .. annotations: 43
adding alternatives:[Acrocraniofacial dysostosis, Kaplan-Plauchu-Fitch syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=949]
processing orphanet number: 65286 ...  .. annotations: 39
adding alternatives:[3q29 microdeletion syndrome, 3q subtelomere deletion syndrome, 3qter deletion, Del(3)(q29), Monosomy 3q29, Monosomy 3qter, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=65286]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 65285 ...  .. annotations: 13
adding alternatives:[Cowden syndrome, Cowden disease, Multiple hamartoma syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=201, Proteus-like syndrome, Cohen-Hayden syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2969, Lhermitte-Duclos disease, Dysplastic gangliocytoma of the cerebellum, LDD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=65285]
processing orphanet number: 65288 ...  .. annotations: 7
adding alternatives:[Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis, Pancreatic and cerebellar agenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=65288]
processing orphanet number: 2232 ...  .. annotations: 9
adding alternatives:[Primary hypergonadotropic hypogonadism - partial alopecia, Al Awadi-Farag-Teebi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2232]
processing orphanet number: 2230 ...  .. annotations: 9
processing orphanet number: 1383 ...  .. annotations: 20
processing orphanet number: 1381 ...  .. annotations: 13
processing orphanet number: 1380 ...  .. annotations: 8
adding alternatives:[Cataract - nephropathy - encephalopathy, Crome syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1380]
processing orphanet number: 2229 ...  .. annotations: 8
adding alternatives:[Dilated cardiomyopathy - hypergonadotropic hypogonadism, Cardiogenital syndrome, Malouf syndrome, Najjar syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2229]
processing orphanet number: 2228 ...  .. annotations: 14
adding alternatives:[Hypodontia - dysplasia of nails, Hypodontia - nail dysgenesis, Tooth and nail syndrome, Witkop syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2228]
processing orphanet number: 2227 ...  .. annotations: 9
processing orphanet number: 79456 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 23480
processing orphanet number: 166272 ...  .. annotations: 23
adding alternatives:[Goldblatt syndrome, Chondrodysplasia - dentinogenesis imperfecta - joint laxity, Goldblatt chondrodysplasia, ODCD, Odontochondrodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166272]
processing orphanet number: 79455 ...  .. annotations: 11
processing orphanet number: 950 ...  .. annotations: 36
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 79458 ...  .. annotations: 2
processing orphanet number: 1377 ...  .. annotations: 9
processing orphanet number: 2224 ...  .. annotations: 19
adding alternatives:[Hypertryptophanemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2224]
processing orphanet number: 79457 ...  .. annotations: 14
adding alternatives:[Maculopapular cutaneous mastocytosis, Urticaria pigmentosa, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79457, Mastocytosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98292]
processing orphanet number: 952 ...  .. annotations: 19
adding alternatives:[Acrofacial dysostosis, Weyers type, Curry-Hall syndrome, Weyers acrodental dysostosis, Weyers acrofacial dysostosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=952]
processing orphanet number: 1376 ...  .. annotations: 5
adding alternatives:[Congenital cataract - ichthyosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1376]
processing orphanet number: 1375 ...  .. annotations: 9
adding alternatives:[Cataract - hypertrichosis - intellectual disability, CAHMR syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1375]
processing orphanet number: 2222 ...  .. annotations: 9
processing orphanet number: 955 ...  .. annotations: 84
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 956 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 957 ...  .. annotations: 13
adding alternatives:[Acropectorovertebral dysplasia, F syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=957]
processing orphanet number: 958 ...  .. annotations: 36
adding alternatives:[Acro-renal-mandibular syndrome, Split hand/split foot - mandibular hypoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=958]
processing orphanet number: 65282 ...  .. annotations: 6
processing orphanet number: 959 ...  .. annotations: 39
adding alternatives:[Acro-renal-ocular syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=959, Okihiro syndrome, Duane-radial ray syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93293]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 261494 ...  .. annotations: 64
adding alternatives:[Kleefstra syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261494]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 157788 ...  .. annotations: 16
adding alternatives:[Hypospadias - hypertelorism - coloboma and deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=157788]
processing orphanet number: 1396 ...  .. annotations: 28
NO OMIMENTRY FOR OMIM-ID 609345 creating NEW one
processing orphanet number: 1394 ...  .. annotations: 35
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1394]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 2241 ...  .. annotations: 18
adding alternatives:[Megacystis-microcolon-intestinal hypoperistalsis syndrome, Berdon syndrome, MMIHS, Megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2241]
processing orphanet number: 1393 ...  .. annotations: 30
adding alternatives:[Cerebro-costo-mandibular syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1393]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 77260 ...  .. annotations: 15
adding alternatives:[Gaucher disease, Acid beta-glucosidase deficiency, Glucocerebrosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355, Gaucher disease type 2, Acute neuronopathic Gaucher disease, Infantile cerebral Gaucher disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=77260]
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 77261 ...  .. annotations: 34
adding alternatives:[Gaucher disease, Acid beta-glucosidase deficiency, Glucocerebrosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355, Gaucher disease type 3, Cerebral juvenile and adult form of Gaucher disease, Chronic neuronopathic Gaucher disease, Gaucher disease, subacute neuronopathic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=77261]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1390 ...  .. annotations: 24
processing orphanet number: 2239 ...  .. annotations: 11
adding alternatives:[Familial isolated hypoparathyroidism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2238, Familial isolated hypoparathyroidism due to agenesis of parathyroid gland, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2239]
processing orphanet number: 2238 ...  .. annotations: 14
processing orphanet number: 2237 ...  .. annotations: 21
adding alternatives:[Hypoparathyroidism - deafness - renal disease, Barakat syndrome, HDR syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2237]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1389 ...  .. annotations: 15
adding alternatives:[Cortical blindness - intellectual disability - polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1389]
processing orphanet number: 1388 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2235 ...  .. annotations: 3
processing orphanet number: 963 ...  .. annotations: 52
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1387 ...  .. annotations: 31
adding alternatives:[Cataract - intellectual disability - hypogonadism, Martsolf syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1387]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2234 ...  .. annotations: 21
adding alternatives:[Male hypergonadotropic hypogonadism - intellectual disability - skeletal anomalies, Sohval-Soffer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2234]
processing orphanet number: 2233 ...  .. annotations: 17
processing orphanet number: 965 ...  .. annotations: 25
adding alternatives:[Acromegaloid facial appearance syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=965]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 966 ...  .. annotations: 14
processing orphanet number: 100024 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 48080
processing orphanet number: 100025 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 968 ...  .. annotations: 18
adding alternatives:[Acromesomelic dysplasia, Hunter-Thomson type, Acromesomelic dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=968]
processing orphanet number: 100026 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 969 ...  .. annotations: 20
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=969]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 157794 ...  .. annotations: 6
processing orphanet number: 261483 ...  .. annotations: 20
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=261483]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 281090 ...  .. annotations: 23
adding alternatives:[Recessive X-linked ichthyosis, RXLI, Steroid sulfatase deficiency, X-linked ichthyosis, XLI, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=461, Syndromic X-linked ichthyosis, Syndromic RXLI, Syndromic recessive X-linked ichthyosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=281090]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 158668 ...  .. annotations: 19
adding alternatives:[Epidermolysis bullosa simplex due to plakophilin deficiency, Ectodermal dysplasia - skin fragility syndrome, McGrath syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=158668]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 101330 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 3101 ...  .. annotations: 10
adding alternatives:[Richieri Costa-da Silva syndrome, Myotonia - intellectual disability - skeletal anomalies, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3101]
processing orphanet number: 2254 ...  .. annotations: 9
processing orphanet number: 2253 ...  .. annotations: 7
adding alternatives:[Foveal hypoplasia - presenile cataract, O'Donnell-Pappas syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2253]
processing orphanet number: 2252 ...  .. annotations: 7
adding alternatives:[Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema, Schmitt-Gillenwater-Kelly syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2252]
processing orphanet number: 2251 ...  .. annotations: 17
adding alternatives:[Thumb deformity - alopecia - pigmentation anomaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2251]
processing orphanet number: 2250 ...  .. annotations: 15
adding alternatives:[Arrhinia - choanal atresia - microphthalmia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1135, Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism, Bosma-Henkin-Christiansen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2250]
processing orphanet number: 79473 ...  .. annotations: 5
adding alternatives:[Porphyria variegata, Protoporphyrinogen oxidase deficiency, Variegate porphyria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79473]
processing orphanet number: 77297 ...  .. annotations: 39
NO OMIMENTRY FOR OMIM-ID 609628 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 79476 ...  .. annotations: 12
adding alternatives:[Griscelli disease, Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Partial albinism - immunodeficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=381, Griscelli disease type 1, Griscelli-Pruniéras syndrome type 1, Hypopigmentation - neurologic impairment, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79476]
processing orphanet number: 77298 ...  .. annotations: 19
adding alternatives:[Anophthalmia/microphthalmia - esophageal atresia, MCOPS3, Syndromic microphthalmia type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=77298]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 970 ...  .. annotations: 15
processing orphanet number: 2249 ...  .. annotations: 16
adding alternatives:[Ulna hypoplasia - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2249]
processing orphanet number: 79478 ...  .. annotations: 3
adding alternatives:[Griscelli disease, Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Partial albinism - immunodeficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=381, Griscelli disease type 3, Griscelli-Pruniéras syndrome type 3, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79478]
processing orphanet number: 2248 ...  .. annotations: 8
processing orphanet number: 971 ...  .. annotations: 10
processing orphanet number: 79477 ...  .. annotations: 21
adding alternatives:[Griscelli disease, Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Partial albinism - immunodeficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=381, Griscelli disease type 2, Griscelli-Pruniéras syndrome type 2, Hypopigmentation - immunodeficiency with or without neurologic impairment, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79477]
processing orphanet number: 972 ...  .. annotations: 9
adding alternatives:[Hereditary continuous muscle fiber activity, Isaacs-Mertens syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=972, Episodic ataxia type 1, Episodic ataxia with myokymia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=37612]
processing orphanet number: 973 ...  .. annotations: 4
adding alternatives:[Congenital absence/hypoplasia of fingers excluding thumb, unilateral, Adactyly of hand, unilateral, Digits 2-5 hypodactyly, unilateral, Digits 2-5 oligodactyly, unilateral, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=973, Congenital absence/hypoplasia of fingers excluding thumb, Digits 2-5 hypodactyly, Digits 2-5 oligodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=294990]
processing orphanet number: 1399 ...  .. annotations: 14
adding alternatives:[Richards-Rundle syndrome, Ketoaciduria - intellectual disability - ataxia - deafness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1399]
processing orphanet number: 2246 ...  .. annotations: 10
adding alternatives:[Cerebellar hypoplasia - tapetoretinal degeneration, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2246]
processing orphanet number: 974 ...  .. annotations: 47
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1398 ...  .. annotations: 10
processing orphanet number: 1397 ...  .. annotations: 5
adding alternatives:[Cerebellum agenesis - hydrocephaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1397]
processing orphanet number: 976 ...  .. annotations: 7
adding alternatives:[Adenine phosphoribosyltransferase deficiency, 2,8-dihydroxyadenine urolithiasis, APRT deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=976]
processing orphanet number: 977 ...  .. annotations: 16
adding alternatives:[Adrenomyodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=977]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 978 ...  .. annotations: 22
adding alternatives:[ADULT syndrome, Acro-dermato-ungual-lacrimal-tooth syndrome, Pigment anomaly - ectrodactyly - hypodontia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=978]
processing orphanet number: 158673 ...  .. annotations: 6
processing orphanet number: 140908 ...  .. annotations: 9
adding alternatives:[Brachydactyly type B2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=140908]
processing orphanet number: 3111 ...  .. annotations: 6
adding alternatives:[Rotor syndrome, Hyperbilirubinemia, Rotor type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3111]
processing orphanet number: 3110 ...  .. annotations: 16
adding alternatives:[Rombo syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3110]
processing orphanet number: 2261 ...  .. annotations: 16
adding alternatives:[Hypospadias - intellectual disability, Goldblatt type, Goldblatt-Wallis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2261]
processing orphanet number: 166277 ...  .. annotations: 10
adding alternatives:[Suarez-Stickler syndrome, Skeletal dysplasia with wormian bone - multiple fractures - dentin abnormality, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=166277]
processing orphanet number: 3109 ...  .. annotations: 5
processing orphanet number: 3107 ...  .. annotations: 61
processing orphanet number: 983 ...  .. annotations: 10
adding alternatives:[Testicular regression syndrome, ETRS, Embryonic testicular regression syndrome, TRS, Vanishing testes syndrome, Vanishing testis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=983]
processing orphanet number: 2258 ...  .. annotations: 4
processing orphanet number: 3105 ...  .. annotations: 12
processing orphanet number: 500 ...  .. annotations: 47
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 2257 ...  .. annotations: 2
adding alternatives:[Familial primary pulmonary hypoplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2257]
processing orphanet number: 3104 ...  .. annotations: 9
adding alternatives:[Robin sequence - oligodactyly, Pierre Robin sequence - oligodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3104]
processing orphanet number: 3103 ...  .. annotations: 48
processing orphanet number: 2256 ...  .. annotations: 25
adding alternatives:[Fibulo-ulnar hypoplasia - renal anomalies, Saito-Kuba-Tsuruta syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2256]
processing orphanet number: 502 ...  .. annotations: 40
adding alternatives:[Langer-Giedion syndrome, Deletion 8q24.1, Monosomy 8q24.1, Trichorhinophalangeal syndrome type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=502]
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2255 ...  .. annotations: 1
adding alternatives:[Pancreatic hypoplasia - diabetes - congenital heart disease, Yorifuji-Okuno syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2255]
processing orphanet number: 3102 ...  .. annotations: 21
adding alternatives:[Richieri Costa-Pereira syndrome, Short stature - Pierre Robin sequence - cleft mandible - hand anomalies clubfoot, Short stature - Pierre Robin syndrome - cleft mandible - hand anomalies clubfoot, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3102]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 503 ...  .. annotations: 27
adding alternatives:[Autosomal dominant Larsen syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=503]
processing orphanet number: 988 ...  .. annotations: 7
adding alternatives:[Absent tibia - polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=988, Hypoplastic tibiae - postaxial polydactyly, Werner mesomelic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3332]
processing orphanet number: 989 ...  .. annotations: 25
adding alternatives:[Hypoglossia-hypodactyly syndrome, Aglossia-adactylia syndrome, Hanhart syndrome, Jussieu syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=989]
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 505 ...  .. annotations: 7
processing orphanet number: 506 ...  .. annotations: 12
adding alternatives:[Leigh syndrome, Infantile subacute necrotizing encephalopathy, Leigh disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=506, Maternally-inherited Leigh syndrome, MILS, Maternally-inherited Leigh disease, Maternally-inherited infantile subacute necrotizing encephalopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=255210, Leigh syndrome with leukodystrophy, Infantile subacute necrotizing encephalopathy with leukodystrophy, Leigh disease with leukodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=255241, Leigh syndrome with cardiomyopathy, Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency, Cardiomyopathy with myopathy due to COX deficiency, Leigh disease with myopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=70474]
  ... no hpo-term mapping for orphanet annotation: 49340
processing orphanet number: 508 ...  .. annotations: 37
adding alternatives:[Leprechaunism, Donohue syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=508]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 100006 ...  .. annotations: 8
adding alternatives:[ABetaA21G amyloidosis, ABetaA21G-related amyloidosis, Beta amyloidosis, Flemish type, HCHWA, Flemish type, Hereditary cerebral hemorrhage with amyloidosis, Flemish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324718, ABeta amyloidosis, Italian type, ABetaE22K amyloidosis, HCHWA, Italian type, Hereditary cerebral hemorrhage with amyloidosis, Italian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324713, ABeta amyloidosis, Arctic type, ABetaE22G amyloidosis, HCHWA, Arctic type, Hereditary cerebral hemorrhage with amyloidosis, Arctic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324723, ABeta amyloidosis, Iowa type, ABetaD23N amyloidosis, HCHWA, Iowa type, Hereditary cerebral hemorrhage with amyloidosis, Iowa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324708, ABetaL34V amyloidosis, ABetaL34V-related amyloidosis, Beta amyloidosis, Piedmont type, HCHWA, Piedmont type, Hereditary cerebral hemorrhage with amyloidosis, Piedmont type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324703, Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ABeta amyloidosis, Dutch type, ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, Hereditary cerebral hemorrhage with amyloidosis, Dutch type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100006]
processing orphanet number: 100008 ...  .. annotations: 5
adding alternatives:[Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ACys amyloidosis, CST3-related amyloidosis, Cystatin amyloidosis, HCHWA, Icelandic type, Hereditary cerebral hemorrhage with amyloidosis, Icelandic type, Hereditary cystatin C amyloid angiopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100008]
processing orphanet number: 217346 ...  .. annotations: 38
adding alternatives:[19q13.11 microdeletion syndrome, Del(19)(q13.11), Monosomy 19q13.11, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=217346]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 163634 ...  .. annotations: 28
NO OMIMENTRY FOR OMIM-ID 614569 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 217340 ...  .. annotations: 25
NO OMIMENTRY FOR OMIM-ID 613533 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 73267 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2274 ...  .. annotations: 8
adding alternatives:[Ichthyosis - hepatosplenomegaly - cerebellar degeneration, Dykes-Markes-Harper syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2274]
processing orphanet number: 3121 ...  .. annotations: 35
adding alternatives:[Ruvalcaba syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3121]
processing orphanet number: 2273 ...  .. annotations: 54
adding alternatives:[Ichthyosis follicularis - alopecia - photophobia, IFAP syndrome, Ichthyosis follicularis - atrichia - photophobia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2273, BRESEK syndrome, BRESHECK syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85284]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 2272 ...  .. annotations: 9
adding alternatives:[Ichthyosis - oral and digital anomalies, Clayton Smith-Donnai syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2272]
  ... no hpo-term mapping for orphanet annotation: 20340
processing orphanet number: 99892 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2271 ...  .. annotations: 8
processing orphanet number: 99893 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 990 ...  .. annotations: 20
adding alternatives:[Agnathia-holoprosencephaly-situs inversus syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=990]
processing orphanet number: 991 ...  .. annotations: 31
NO OMIMENTRY FOR OMIM-ID 202660 creating NEW one
processing orphanet number: 510 ...  .. annotations: 11
processing orphanet number: 994 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 26680
processing orphanet number: 2269 ...  .. annotations: 13
adding alternatives:[Ichthyosis - alopecia - eclabion - ectropion - intellectual disability, Jagell-Holmgren-Hofer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2269]
processing orphanet number: 34587 ...  .. annotations: 6
adding alternatives:[Glycogen storage disease due to LAMP-2 deficiency, Danon disease, GSD due to LAMP-2 deficiency, Glycogenosis due to LAMP-2 deficiency, Lysosomal glycogen storage disease with normal acid maltase activity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=34587]
processing orphanet number: 511 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 23030
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2268 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 52600
processing orphanet number: 3115 ...  .. annotations: 6
adding alternatives:[Roussy-Lévy syndrome, Hereditary areflexic dystasia, Roussy-Lévy type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3115]
processing orphanet number: 512 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 49500
processing orphanet number: 2267 ...  .. annotations: 11
adding alternatives:[Ichthyosis-cheek-eyebrow syndrome, Sidransky-Feinstein-Goodman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2267]
  ... no hpo-term mapping for orphanet annotation: 3560
processing orphanet number: 998 ...  .. annotations: 7
adding alternatives:[Albinism-deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=998]
processing orphanet number: 999 ...  .. annotations: 16
adding alternatives:[Ermine phenotype, O'Doherty syndrome, Pigmentary disorder with hearing loss, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=999]
processing orphanet number: 100073 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 99889 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 99888 ...  .. annotations: 7
processing orphanet number: 97229 ...  .. annotations: 34
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2287 ...  .. annotations: 3
adding alternatives:[Fused mandibular incisors, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2287]
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 3134 ...  .. annotations: 32
adding alternatives:[SCARF syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3134]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 2286 ...  .. annotations: 37
adding alternatives:[Holoprosencephaly, HPE, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2162, Solitary median maxillary central incisor syndrome, SMMCI, Single upper central incisor, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2286, Microform holoprosencephaly, Microform HPE, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=280200]
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 3133 ...  .. annotations: 10
adding alternatives:[Say-Field-Coldwell syndrome, Triphalangeal thumbs - dislocation of patella, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3133]
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 2285 ...  .. annotations: 7
adding alternatives:[Primary basilar invagination, Bull-Nixon syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2285]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 3132 ...  .. annotations: 33
adding alternatives:[Say-Barber-Miller syndrome, Microcephaly - hypogammaglobulinemia - abnormal immunity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3132]
processing orphanet number: 3130 ...  .. annotations: 20
adding alternatives:[Satoyoshi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3130]
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 73273 ...  .. annotations: 14
adding alternatives:[Growth delay due to insulin-like growth factor I resistance, Resistance to IGF-1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=73273]
  ... no hpo-term mapping for orphanet annotation: 52000
processing orphanet number: 2282 ...  .. annotations: 32
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3128 ...  .. annotations: 11
adding alternatives:[Sakati-Nyhan syndrome, ACPS III, ACPS with leg hypoplasia, Acrocephalopolysyndactyly type 3, Sakati syndrome, Sakati-Nyhan-Tisdale syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3128]
processing orphanet number: 226295 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2278 ...  .. annotations: 10
adding alternatives:[Ichthyosis - intellectual disability - dwarfism - renal impairment, Passwell-Goodman-Siprkowski syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2278]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 523 ...  .. annotations: 10
adding alternatives:[Hereditary leiomyomatosis and renal cell cancer, Familial leiomyomatosis and renal cell cancer, Familial leiomyomatosis cutis et uteri, Familial leiomyomatosis with renal carcinoma, Familial multiple cutaneous leiomyomas, HLRCC, Hereditary leiomyomatosis, Hereditary leiomyomatosis with renal carcinoma, Hereditary multiple cutaneous leiomyomas, MCUL, Multiple cutaneous and uterine leiomyomas, Reed syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=523]
  ... no hpo-term mapping for orphanet annotation: 26200
processing orphanet number: 524 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 50070
processing orphanet number: 226298 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 525 ...  .. annotations: 17
processing orphanet number: 526 ...  .. annotations: 10
adding alternatives:[Liddle syndrome, Pseudoaldosteronism, Pseudohyperaldosteronism type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=526]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 226292 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 528 ...  .. annotations: 45
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 529 ...  .. annotations: 2
processing orphanet number: 2290 ...  .. annotations: 3
adding alternatives:[Microvillus inclusion disease, Congenital microvillous atrophy, Congenital microvillus atrophy, MVID, Microvillous inclusion disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2290]
processing orphanet number: 284160 ...  .. annotations: 40
adding alternatives:[8q21.11 microdeletion syndrome, Del(8)(q21.11), Deletion 8q21.11, Monosomy 8q21.11, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=284160]
processing orphanet number: 3145 ...  .. annotations: 13
adding alternatives:[Nephrogenic diabetes insipidus - intracranial calcification, Schofer-Beetz-Bohl syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3145]
processing orphanet number: 2297 ...  .. annotations: 9
NO OMIMENTRY FOR OMIM-ID 610549 creating NEW one
processing orphanet number: 3144 ...  .. annotations: 24
adding alternatives:[Schneckenbecken dysplasia, Chondrodysplasia with snail-like pelvis, SLC35D1-CDG, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3144]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 3143 ...  .. annotations: 9
adding alternatives:[Autoimmune polyendocrinopathy type 2, APS type 2, APS2, Autoimmune polyendocrine syndrome type 2, Autoimmune polyglandular syndrome type 2, Autoimmune thyroid disease and/or type 1 diabetes - Addison disease, Schmidt syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3143]
processing orphanet number: 2295 ...  .. annotations: 9
adding alternatives:[Ehlers-Danlos syndrome type 11, EDS XI, Familial joint instability syndrome, Familial joint laxity, Joint instability syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2295]
processing orphanet number: 2292 ...  .. annotations: 2
processing orphanet number: 2291 ...  .. annotations: 5
adding alternatives:[Congenital velopharyngeal incompetence, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2291]
processing orphanet number: 530 ...  .. annotations: 24
adding alternatives:[Lipoid proteinosis, Hyalinosis cutis et mucosae, Urbach-Wiethe disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=530]
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 531 ...  .. annotations: 18
adding alternatives:[Miller-Dieker syndrome, Lissencephaly due to 17p13.3 deletion, Monosomy 17p13.3, Telomeric deletion 17p, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=531]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3138 ...  .. annotations: 38
adding alternatives:[Ulnar-mammary syndrome, Schinzel syndrome, UMS, Ulnar-mammary syndrome of Pallister, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3138]
processing orphanet number: 3137 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 23600
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 534 ...  .. annotations: 122
adding alternatives:[Oculocerebrorenal syndrome, Lowe disease, Lowe oculo-cerebro-renal syndrome, Lowe syndrome, OCR, OCRL, Oculo-cerebro-renal dystrophy, Oculo-cerebro-renal syndrome, Oculocerebrorenal dystrophy, Phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=534]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 49020
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 2289 ...  .. annotations: 18
NO OMIMENTRY FOR OMIM-ID 603472 creating NEW one
processing orphanet number: 535 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 23070
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 23490
processing orphanet number: 3135 ...  .. annotations: 3
adding alternatives:[Familial Scheuermann disease, Familial Scheuermann juvenile kyphosis, Familial spinal osteochondrosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3135]
processing orphanet number: 536 ...  .. annotations: 99
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 23070
  ... no hpo-term mapping for orphanet annotation: 23490
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 85277 ...  .. annotations: 16
adding alternatives:[X-linked intellectual disability, Cantagrel type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85277]
processing orphanet number: 537 ...  .. annotations: 42
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 40540
processing orphanet number: 85276 ...  .. annotations: 35
adding alternatives:[X-linked intellectual disability, Armfield type, Armfield syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85276]
processing orphanet number: 538 ...  .. annotations: 36
adding alternatives:[Lymphangioleiomyomatosis, LAM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=538]
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 23710
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 85279 ...  .. annotations: 23
adding alternatives:[Syndromic X-linked intellectual disability due to JARID1C mutation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85279]
processing orphanet number: 85278 ...  .. annotations: 37
adding alternatives:[Christianson syndrome, X-linked Angelman-like syndrome, X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy, X-linked intellectual disability, South African type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85278]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 85273 ...  .. annotations: 15
adding alternatives:[X-linked intellectual disability, Abidi type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85273]
processing orphanet number: 85275 ...  .. annotations: 4
adding alternatives:[Microphthalmia - ankyloblepharon - intellectual disability, MCOPS4, Syndromic microphthalmia type 4, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85275]
processing orphanet number: 85274 ...  .. annotations: 14
adding alternatives:[Syndromic X-linked intellectual disability 7, MRXS7, X-linked intellectual disability, Ahmad type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85274]
processing orphanet number: 46532 ...  .. annotations: 6
processing orphanet number: 217377 ...  .. annotations: 12
adding alternatives:[Microduplication Xp11.22-p11.23 syndrome, Trisomy Xp11.22-p11.23, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=217377]
processing orphanet number: 99429 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 3156 ...  .. annotations: 15
processing orphanet number: 3152 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 3151 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 33226 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 48080
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 53693 ...  .. annotations: 11
adding alternatives:[GRACILE syndrome, Fellman disease, Growth delay - aminoaciduria - cholestasis - iron overload - lactic acidosis - early death, Growth restriction - aminoaciduria - cholestasis - iron overload - lactic acidosis - early death, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=53693]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 542 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 53697 ...  .. annotations: 10
adding alternatives:[Gnathodiaphyseal dysplasia, GDD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=53697]
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 545 ...  .. annotations: 14
adding alternatives:[Follicular lymphoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=545]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 48080
processing orphanet number: 549 ...  .. annotations: 42
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 65682 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 27420
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 85291 ...  .. annotations: 37
adding alternatives:[X-linked intellectual disability, Wittwer type, Wittwer syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85291]
  ... no hpo-term mapping for orphanet annotation: 3240
processing orphanet number: 65684 ...  .. annotations: 13
adding alternatives:[Monomelic amyotrophy, Benign focal amyotrophy, Hirayama disease, JMADUE, Juvenile muscular atrophy of distal upper extremity, Juvenile muscular atrophy of the distal upper limb, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=65684]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 85293 ...  .. annotations: 23
adding alternatives:[X-linked intellectual disability, Cabezas type, Cabezas syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85293]
processing orphanet number: 217385 ...  .. annotations: 19
NO OMIMENTRY FOR OMIM-ID 613215 creating NEW one
processing orphanet number: 3167 ...  .. annotations: 9
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3165 ...  .. annotations: 18
adding alternatives:[Eosinophilic fasciitis, Diffuse fasciitis with eosinophilia, Shulman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3165]
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 44600
processing orphanet number: 3164 ...  .. annotations: 22
adding alternatives:[Omphalocele syndrome, Shprintzen-Goldberg type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3164]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3163 ...  .. annotations: 40
adding alternatives:[SHORT syndrome, Aarskog-Ose-Pande syndrome, Lipodystrophy - Rieger anomaly - diabetes, Rieger anomaly - partial lipodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3163]
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 3162 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 550 ...  .. annotations: 118
adding alternatives:[MELAS, Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes, Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=550]
  ... no hpo-term mapping for orphanet annotation: 49340
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 38160
  ... no hpo-term mapping for orphanet annotation: 43260
  ... no hpo-term mapping for orphanet annotation: 49020
processing orphanet number: 551 ...  .. annotations: 11
adding alternatives:[MERRF, Fukuhara syndrome, Myoclonus epilepsy associated with ragged-red fibers, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=551]
processing orphanet number: 55881 ...  .. annotations: 21
adding alternatives:[Adamantinoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=55881]
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 553 ...  .. annotations: 41
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 556 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 23490
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 3157 ...  .. annotations: 34
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3157, Combined pituitary hormone deficiencies, genetic forms, Familial congenital hypopituitarism, Multiple pituitary hormone deficiencies, genetic forms, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=95494]
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 55540
processing orphanet number: 558 ...  .. annotations: 48
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 46760
processing orphanet number: 140952 ...  .. annotations: 28
NO OMIMENTRY FOR OMIM-ID 300707 creating NEW one
processing orphanet number: 559 ...  .. annotations: 27
adding alternatives:[Marinesco-Sjögren syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=559]
processing orphanet number: 85295 ...  .. annotations: 4
adding alternatives:[HSD10 disease, atypical type, HSD10 deficiency, atypical type, Syndromic X-linked intellectual disability type 10, X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85295]
processing orphanet number: 85294 ...  .. annotations: 5
adding alternatives:[X-linked epilepsy - learning disabilities - behavior disorders, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85294]
processing orphanet number: 85297 ...  .. annotations: 6
adding alternatives:[X-linked spinocerebellar ataxia type 3, SCAX3, X-linked ataxia-deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85297]
processing orphanet number: 85280 ...  .. annotations: 17
adding alternatives:[X-linked intellectual disability - cubitus valgus - dysmorphism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85280]
processing orphanet number: 85282 ...  .. annotations: 24
NO OMIMENTRY FOR OMIM-ID 300148 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3177 ...  .. annotations: 16
adding alternatives:[Corneal-cerebellar syndrome, Der Kaloustian-Jarudi-Khoury syndrome, Spinocerebellar degeneration - corneal dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3177]
processing orphanet number: 3176 ...  .. annotations: 3
processing orphanet number: 3175 ...  .. annotations: 4
adding alternatives:[Early infantile epileptic encephalopathy, EIEE, Early infantile epileptic encephalopathy with suppression-bursts, Ohtahara syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1934, West syndrome, Infantile spasms, Intellectual disability - hypsarrhythmia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3451, Spasticity - intellectual disability - X-linked epilepsy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3175, Infantile epileptic-dyskinetic encephalopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=364063]
processing orphanet number: 75497 ...  .. annotations: 12
adding alternatives:[X-linked Ehlers-Danlos syndrome, EDS V, Ehlers-Danlos syndrome type 5, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=75497]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 217390 ...  .. annotations: 14
adding alternatives:[Autosomal recessive hyper-IgE syndrome, AR-HIES, Autosomal recessive HIES, Hyperimmunoglobulin E syndrome type 2, Non-skeletal hyper-IgE syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=169446, Combined immunodeficiency due to DOCK8 deficiency, CID due to DOCK8 deficiency, Combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency, DOCK8 immunodeficiency syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=217390]
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 75496 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 3173 ...  .. annotations: 16
processing orphanet number: 3172 ...  .. annotations: 9
adding alternatives:[Eyebrow duplication - syndactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3172]
processing orphanet number: 560 ...  .. annotations: 41
adding alternatives:[Marshall syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=560]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 561 ...  .. annotations: 36
adding alternatives:[Marshall-Smith syndrome, Accelerated skeletal maturation - peculiar facies - failure to thrive, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=561]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 562 ...  .. annotations: 35
adding alternatives:[McCune-Albright syndrome, Gonadotropin-independent female-limited sexual precocity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=562]
processing orphanet number: 564 ...  .. annotations: 45
processing orphanet number: 565 ...  .. annotations: 57
adding alternatives:[Menkes disease, Kinky hair disease, Kinky hair syndrome, MD, MK, MNK, Menkes syndrome, Steely hair disease, Steely hair syndrome, Trichopoliodystrophy, X-linked copper deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=565]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 567 ...  .. annotations: 98
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 3169 ...  .. annotations: 11
adding alternatives:[Sirenomelia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3169, Caudal regression sequence, Caudal dysplasia, Sacral agenesis syndrome, Sacral regression syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3027, Familial caudal dysgenesis, Rudd-Klimek syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1768]
processing orphanet number: 568 ...  .. annotations: 43
processing orphanet number: 3168 ...  .. annotations: 12
adding alternatives:[Sillence syndrome, Brachydactyly-symphalangism syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3168]
processing orphanet number: 569 ...  .. annotations: 9
processing orphanet number: 85287 ...  .. annotations: 13
adding alternatives:[X-linked intellectual disability, Siderius type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85287]
processing orphanet number: 85289 ...  .. annotations: 27
adding alternatives:[X-linked intellectual disability, Vitale type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85289]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 140966 ...  .. annotations: 4
adding alternatives:[Palmoplantar keratoderma, Nagashima type, PPK, Nagashima type, Palmoplantar hyperkeratosis, Nagashima type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=140966]
processing orphanet number: 33208 ...  .. annotations: 2
processing orphanet number: 85284 ...  .. annotations: 31
adding alternatives:[Ichthyosis follicularis - alopecia - photophobia, IFAP syndrome, Ichthyosis follicularis - atrichia - photophobia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2273, BRESEK syndrome, BRESHECK syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85284]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 85283 ...  .. annotations: 10
adding alternatives:[X-linked intellectual disability, Miles-Carpenter type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85283]
processing orphanet number: 85286 ...  .. annotations: 13
adding alternatives:[X-linked intellectual disability, Shashi type, Syndromic X-linked intellectual disability type 11, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85286]
processing orphanet number: 3181 ...  .. annotations: 3
adding alternatives:[Sprengel deformity, High scapula, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3181]
processing orphanet number: 3180 ...  .. annotations: 4
adding alternatives:[Spondylocamptodactyly syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3180]
processing orphanet number: 231230 ...  .. annotations: 6
processing orphanet number: 3189 ...  .. annotations: 3
adding alternatives:[Congenital pulmonary valve stenosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3189]
processing orphanet number: 3188 ...  .. annotations: 4
processing orphanet number: 3186 ...  .. annotations: 29
adding alternatives:[Holoprosencephaly - radial heart renal anomalies, Steinfeld syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3186]
processing orphanet number: 3185 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 3184 ...  .. annotations: 7
adding alternatives:[Steatocystoma multiplex - natal teeth, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3184]
processing orphanet number: 570 ...  .. annotations: 43
adding alternatives:[Moebius syndrome, Congenital facial diplegia, Möbius syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=570]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 183660 ...  .. annotations: 21
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 97297 ...  .. annotations: 52
adding alternatives:[Bohring-Opitz syndrome, BOS syndrome, Bohring syndrome, C-like syndrome, Oberklaid-Danks syndrome, Opitz trigonocephaly-like syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97297]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 573 ...  .. annotations: 18
adding alternatives:[Monilethrix, Moniliform hair syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=573]
processing orphanet number: 575 ...  .. annotations: 36
adding alternatives:[Muckle-Wells syndrome, Neutrophilic urticaria, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=575]
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 576 ...  .. annotations: 29
adding alternatives:[Mucolipidosis type II, I-cell disease, N-acetylglucosamine 1-phosphotransferase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=576]
  ... no hpo-term mapping for orphanet annotation: 49500
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 577 ...  .. annotations: 23
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 578 ...  .. annotations: 26
adding alternatives:[Mucolipidosis type IV, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=578]
  ... no hpo-term mapping for orphanet annotation: 49500
processing orphanet number: 579 ...  .. annotations: 58
  ... no hpo-term mapping for orphanet annotation: 20160
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 231222 ...  .. annotations: 12
adding alternatives:[Beta-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=848, Beta-thalassemia intermedia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231222, Beta-thalassemia major, Cooley anemia, Mediterranean anemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231214]
processing orphanet number: 231226 ...  .. annotations: 6
NO OMIMENTRY FOR OMIM-ID 603902 creating NEW one
processing orphanet number: 3191 ...  .. annotations: 25
adding alternatives:[Subaortic stenosis - short stature, Onat syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3191]
processing orphanet number: 90650 ...  .. annotations: 24
adding alternatives:[Otopalatodigital syndrome, Taybi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=669, Otopalatodigital syndrome type 1, OPD I syndrome, OPD syndrome 1, Taybi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90650]
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 90653 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 90652 ...  .. annotations: 43
adding alternatives:[Otopalatodigital syndrome, Taybi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=669, Otopalatodigital syndrome type 2, OPD II syndrome, OPD syndrome 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90652]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 90654 ...  .. annotations: 8
adding alternatives:[Stickler syndrome, Hereditary progressive arthroophthalmopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=828, Stickler syndrome type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90654]
processing orphanet number: 3199 ...  .. annotations: 10
adding alternatives:[Stimmler syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3199]
processing orphanet number: 3197 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 3196 ...  .. annotations: 3
processing orphanet number: 580 ...  .. annotations: 35
adding alternatives:[Mucopolysaccharidosis type 2, Hunter syndrome, Iduronate 2-sulfatase deficiency, MPS2, MPSII, Mucopolysaccharidosis type II, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=580]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 3195 ...  .. annotations: 15
processing orphanet number: 581 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 3194 ...  .. annotations: 18
adding alternatives:[Stern-Lubinsky-Durrie syndrome, Corneo-dermato-osseous syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3194]
processing orphanet number: 97286 ...  .. annotations: 12
adding alternatives:[Carney-Stratakis syndrome, Carney dyad, Carney-Stratakis dyad, GIST-paraganglioma dyad, Paraganglioma and gastric stromal sarcoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97286]
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 582 ...  .. annotations: 35
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 3193 ...  .. annotations: 1
adding alternatives:[Supravalvular aortic stenosis, SVAS, Supravalvar aortic stenosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3193]
processing orphanet number: 583 ...  .. annotations: 27
adding alternatives:[Mucopolysaccharidosis type 6, ARSB deficiency, ASB deficiency, Arylsulfatase B deficiency, MPS6, MPSVI, Maroteaux-Lamy disease, Mucopolysaccharidosis type VI, N-acetylgalactosamine 4-sulfatase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=583]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 584 ...  .. annotations: 28
adding alternatives:[Mucopolysaccharidosis type 7, Beta-glucuronidase deficiency, MPS7, MPSVII, Mucopolysaccharidosis type VII, Sly disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=584]
  ... no hpo-term mapping for orphanet annotation: 45930
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 100 ...  .. annotations: 39
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 585 ...  .. annotations: 31
adding alternatives:[Multiple sulfatase deficiency, Austin type juvenile sulfatidosis, MSD, Mucosulfatidosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=585]
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 586 ...  .. annotations: 9
adding alternatives:[Cystic fibrosis, CF, Mucoviscidosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=586]
processing orphanet number: 587 ...  .. annotations: 14
adding alternatives:[Muir-Torre syndrome, Multiple keratoacanthoma, Muir-Torre type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=587]
processing orphanet number: 588 ...  .. annotations: 24
processing orphanet number: 107 ...  .. annotations: 17
processing orphanet number: 108 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 109 ...  .. annotations: 66
adding alternatives:[Bannayan-Riley-Ruvalcaba syndrome, BRRS, Myhre-Riley-Smith syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=109]
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 231214 ...  .. annotations: 48
adding alternatives:[Beta-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=848, Beta-thalassemia intermedia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231222, Beta-thalassemia major, Cooley anemia, Mediterranean anemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231214]
processing orphanet number: 99817 ...  .. annotations: 55
adding alternatives:[Constitutional mismatch repair deficiency syndrome, CMMR-D syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=252202, Non-polyposis Turcot syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99817]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43500
processing orphanet number: 99812 ...  .. annotations: 34
NO OMIMENTRY FOR OMIM-ID 606593 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 63862 ...  .. annotations: 13
processing orphanet number: 93271 ...  .. annotations: 36
processing orphanet number: 163596 ...  .. annotations: 13
adding alternatives:[Hb Bart's hydrops fetalis, Alpha-thalassemia hydrops fetalis, Alpha-thalassemia major, Hemoglobin Bart's hydrops fetalis, Homozygous alpha0-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163596, Hydrops fetalis, Fetal anasarca, Fetal hydrops, Generalized fetal edema, HF, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1041, Non-immune hydrops fetalis, Non-immune HF, Non-immune fetal edema, Non-immune fetal hydrops, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=363999]
processing orphanet number: 592 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 93274 ...  .. annotations: 36
processing orphanet number: 110 ...  .. annotations: 26
processing orphanet number: 111 ...  .. annotations: 5
adding alternatives:[Barth syndrome, 3-methylglutaconic aciduria type 2, BTHS, Cardioskeletal myopathy with neutropenia and abnormal mitochondria, Cardioskeletal myopathy-neutropenia, MGA2, X-linked cardioskeletal myopathy and neutropenia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=111]
processing orphanet number: 595 ...  .. annotations: 15
processing orphanet number: 112 ...  .. annotations: 4
processing orphanet number: 596 ...  .. annotations: 16
adding alternatives:[X-linked centronuclear myopathy, Myotubular myopathy, XLCNM, XLMTM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=596]
processing orphanet number: 597 ...  .. annotations: 4
adding alternatives:[Central core disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=597, Multiminicore myopathy, MmD, Multiminicore disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=598, Moderate multiminicore disease with hand involvement, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=178145]
processing orphanet number: 113 ...  .. annotations: 12
adding alternatives:[Bazex-Dupré-Christol syndrome, BDCS, Follicular atrophoderma and basal cell carcinomas, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=113]
processing orphanet number: 139491 ...  .. annotations: 11
NO OMIMENTRY FOR OMIM-ID 606069 creating NEW one
processing orphanet number: 598 ...  .. annotations: 8
processing orphanet number: 114 ...  .. annotations: 11
adding alternatives:[Auriculoosteodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=114]
processing orphanet number: 115 ...  .. annotations: 21
adding alternatives:[Congenital contractural arachnodactyly, Beals syndrome, Beals-Hecht syndrome, CCA syndrome, Distal arthrogryposis type 9, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=115]
processing orphanet number: 599 ...  .. annotations: 2
processing orphanet number: 116 ...  .. annotations: 38
adding alternatives:[Beckwith-Wiedemann syndrome, BWS, Exomphalos - macroglossia - gigantism, Wiedemann-Beckwith syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=116]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 55700
processing orphanet number: 117 ...  .. annotations: 67
adding alternatives:[Behçet disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=117]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 27660
processing orphanet number: 118 ...  .. annotations: 7
adding alternatives:[Beta-mannosidosis, Beta-mannosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=118]
processing orphanet number: 231242 ...  .. annotations: 4
processing orphanet number: 83473 ...  .. annotations: 15
processing orphanet number: 139498 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 231249 ...  .. annotations: 4
processing orphanet number: 93267 ...  .. annotations: 29
NO OMIMENTRY FOR OMIM-ID 607161 creating NEW one
processing orphanet number: 99803 ...  .. annotations: 19
adding alternatives:[Ondine syndrome, CCHS, Central congenital hypoventilation syndrome, Congenital central alveolar hypoventilation syndrome, Ondine curse, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=661, Haddad syndrome, Congenital central alveolar hypoventilation - Hirschsprung disease, Ondine-Hirschsprung disease, Ondine-Hirschsprung syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99803]
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 93260 ...  .. annotations: 39
processing orphanet number: 71493 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 35720
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 247604 ...  .. annotations: 16
adding alternatives:[Juvenile primary lateral sclerosis, JPLS, Juvenile PLS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=247604]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 120 ...  .. annotations: 51
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43180
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 93262 ...  .. annotations: 29
adding alternatives:[Crouzon syndrome - acanthosis nigricans, Crouzon-dermoskeletal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93262]
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 122 ...  .. annotations: 12
adding alternatives:[Birt-Hogg-Dubé syndrome, Fibrofolliculomas with trichodiscomas and acrochordons, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=122]
  ... no hpo-term mapping for orphanet annotation: 23740
processing orphanet number: 83469 ...  .. annotations: 19
processing orphanet number: 123 ...  .. annotations: 7
adding alternatives:[Björnstad syndrome, Deafness - pili torti - hypogonadism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=123]
processing orphanet number: 124 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 125 ...  .. annotations: 40
adding alternatives:[Bloom syndrome, BSyn, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=125]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 36237 ...  .. annotations: 7
processing orphanet number: 126 ...  .. annotations: 11
adding alternatives:[Blepharophimosis - epicanthus inversus - ptosis, Blepharophimosis types 1 and 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=126]
processing orphanet number: 83465 ...  .. annotations: 4
processing orphanet number: 127 ...  .. annotations: 35
adding alternatives:[Borjeson-Forssman-Lehmann syndrome, BFLS, Intellectual deficiency - epilepsy - endocrine disorders, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=127]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 129 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 83461 ...  .. annotations: 3
adding alternatives:[Congenital primary aphakia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=83461]
processing orphanet number: 231237 ...  .. annotations: 3
adding alternatives:[Hereditary persistence of fetal hemoglobin - sickle cell disease, HPFH - sickle cell disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251380, Delta-beta-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231237, Hereditary persistence of fetal hemoglobin - beta-thalassemia, HPFH - beta-thalassemia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46532]
processing orphanet number: 93299 ...  .. annotations: 28
adding alternatives:[Achondrogenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=932, Achondrogenesis type 1A, Achondrogenesis, Houston-Harris type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93299]
processing orphanet number: 48686 ...  .. annotations: 8
processing orphanet number: 99832 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 254351 ...  .. annotations: 12
NO OMIMENTRY FOR OMIM-ID 613729 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 93298 ...  .. annotations: 28
adding alternatives:[Achondrogenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=932, Achondrogenesis type 1B, Achondrogenesis, Parenti-Fraccaro type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93298]
processing orphanet number: 93296 ...  .. annotations: 25
adding alternatives:[Achondrogenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=932, Achondrogenesis type 2, Achondrogenesis, Langer-Saldino type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93296, Hypochondrogenesis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93297]
processing orphanet number: 131 ...  .. annotations: 20
adding alternatives:[Budd-Chiari syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=131]
  ... no hpo-term mapping for orphanet annotation: 35720
processing orphanet number: 357154 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 50070
processing orphanet number: 254346 ...  .. annotations: 56
  ... no hpo-term mapping for orphanet annotation: 52480
processing orphanet number: 136 ...  .. annotations: 33
adding alternatives:[CADASIL, Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, Hereditary multi-infarct dementia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=136]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 137 ...  .. annotations: 27
  ... no hpo-term mapping for orphanet annotation: 29420
  ... no hpo-term mapping for orphanet annotation: 49400
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 138 ...  .. annotations: 119
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=138]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 32600
processing orphanet number: 139 ...  .. annotations: 44
adding alternatives:[CHILD syndrome, CHILD nevus, Congenital hemidysplasia with ichthyosiform nevus and limbs defects, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139]
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 30925 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 54210
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 168829 ...  .. annotations: 9
processing orphanet number: 99827 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99826 ...  .. annotations: 22
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99829 ...  .. annotations: 30
processing orphanet number: 99828 ...  .. annotations: 23
NO OMIMENTRY FOR OMIM-ID 614371 creating NEW one
processing orphanet number: 99825 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 1809 ...  .. annotations: 19
processing orphanet number: 64741 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 99824 ...  .. annotations: 30
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 93283 ...  .. annotations: 8
adding alternatives:[Spondyloepiphyseal dysplasia, Kimberley type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93283]
processing orphanet number: 140 ...  .. annotations: 38
processing orphanet number: 141 ...  .. annotations: 19
adding alternatives:[Canavan disease, ACY2 deficiency, Aminoacylase 2 deficiency, Aspartoacylase deficiency, Spongy degeneration of the brain, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=141]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 93284 ...  .. annotations: 18
processing orphanet number: 144 ...  .. annotations: 24
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 147 ...  .. annotations: 7
adding alternatives:[Carbamoyl-phosphate synthase deficiency, CPS1 deficiency, Carbamoyl-phosphate synthase 1 deficiency, Carbamoyl-phosphate synthetase 1 deficiency, Carbamoyl-phosphate synthetase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=147]
processing orphanet number: 168811 ...  .. annotations: 10
processing orphanet number: 148 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1808 ...  .. annotations: 9
adding alternatives:[Hidrotic ectodermal dysplasia, Christianson-Fourie type, Christianson-Fourie syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1808]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1807 ...  .. annotations: 25
adding alternatives:[Focal facial dermal dysplasia type III, FFDD type III, FFDD3, Focal facial dermal dysplasia 3, Setleis type, Setleis syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1807, Focal facial dermal dysplasia, FFDD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=398166]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 168816 ...  .. annotations: 8
  ... no hpo-term mapping for orphanet annotation: 40540
processing orphanet number: 1806 ...  .. annotations: 26
adding alternatives:[Ectodermal dysplasia - blindness, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1806]
processing orphanet number: 1803 ...  .. annotations: 19
adding alternatives:[Thoracomelic dysplasia, Rivera-Perez-Salas syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1803]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 1802 ...  .. annotations: 13
adding alternatives:[Ghosal hematodiaphyseal dysplasia, Diaphyseal dysplasia - anemia, Ghosal syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1802]
  ... no hpo-term mapping for orphanet annotation: 45930
processing orphanet number: 1801 ...  .. annotations: 18
adding alternatives:[Kyphomelic dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1801]
processing orphanet number: 46488 ...  .. annotations: 8
processing orphanet number: 46489 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 46486 ...  .. annotations: 9
adding alternatives:[Mucous membrane pemphigoid, Cicatricial pemphigoid, Mucosal pemphigoid, Mucosynechial pemphigoid, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46486]
processing orphanet number: 46487 ...  .. annotations: 11
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 64755 ...  .. annotations: 15
adding alternatives:[Becker nevus syndrome, Pigmentary hairy epidermal nevus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=64755]
processing orphanet number: 64754 ...  .. annotations: 16
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 95496 ...  .. annotations: 15
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 73220 ...  .. annotations: 20
adding alternatives:[X-linked intellectual disability - hypotonic face, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=73220, Renier-Gabreels-Jasper syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93975, Smith-Fineman-Myers syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93974, Chudley-Lowry-Hoar syndrome, Chudley-Lowry syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93971, Holmes-Gang syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93970, Carpenter-Waziri syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93973, Juberg-Marsidi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93972]
processing orphanet number: 221008 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 154 ...  .. annotations: 13
processing orphanet number: 1811 ...  .. annotations: 6
adding alternatives:[Odontomicronychial dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1811]
processing orphanet number: 155 ...  .. annotations: 4
  ... no hpo-term mapping for orphanet annotation: 52600
processing orphanet number: 1810 ...  .. annotations: 18
processing orphanet number: 156 ...  .. annotations: 19
adding alternatives:[Carnitine palmitoyl transferase 1A deficiency, CPT1A deficiency, Carnitine palmitoyl transferase IA deficiency, Hepatic carnitine palmitoyl transferase 1 deficiency, Hepatic carnitine palmitoyl transferase I deficiency, L-CPT1 deficiency, L-CPTI deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=156]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 157 ...  .. annotations: 20
processing orphanet number: 36204 ...  .. annotations: 18
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 87876 ...  .. annotations: 29
processing orphanet number: 1819 ...  .. annotations: 20
processing orphanet number: 1818 ...  .. annotations: 13
adding alternatives:[Ectodermal dysplasia, trichoodontoonychial type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1818]
processing orphanet number: 46485 ...  .. annotations: 4
processing orphanet number: 1816 ...  .. annotations: 17
adding alternatives:[Ectodermal dysplasia, Berlin type, Leukomelanoderma - intellectual disability - hypotrichosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1816]
processing orphanet number: 85212 ...  .. annotations: 16
adding alternatives:[Gaucher disease, Acid beta-glucosidase deficiency, Glucocerebrosidase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355, Fetal Gaucher disease, Perinatal lethal Gaucher disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85212]
processing orphanet number: 139450 ...  .. annotations: 5
adding alternatives:[Microtia-eye coloboma-imperforation of the nasolacrimal duct, Balikova-Vermeesch syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139450]
processing orphanet number: 1812 ...  .. annotations: 39
adding alternatives:[Ectodermal dysplasia - intellectual disability - central nervous system malformation, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1812]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 352723 ...  .. annotations: 16
processing orphanet number: 160 ...  .. annotations: 35
adding alternatives:[Castleman disease, Angiofollicular ganglionic hyperplasia, Angiofollicular lymph hyperplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=160, Kaposi sarcoma, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=33276, Multicentric Castleman disease, MCD, Multicentric giant lymph node hyperplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93686]
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 38160
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 163 ...  .. annotations: 2
adding alternatives:[Hereditary hyperferritinemia with congenital cataracts, Bonneau-Beaumont syndrome, HHCS, Hereditary hyperferritinemia-cataract syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=163]
processing orphanet number: 164 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 1822 ...  .. annotations: 13
adding alternatives:[Dysplasia epiphysealis hemimelica, Trevor disease, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1822]
processing orphanet number: 165 ...  .. annotations: 29
  ... no hpo-term mapping for orphanet annotation: 29420
processing orphanet number: 166 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 20240
processing orphanet number: 167 ...  .. annotations: 40
adding alternatives:[Chédiak-Higashi syndrome, Chédiak-Higashi disease, Chédiak-Higashi-Steinbrink syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=167]
  ... no hpo-term mapping for orphanet annotation: 48080
processing orphanet number: 168 ...  .. annotations: 4
adding alternatives:[Loose anagen syndrome, Coloboma - hair abnormality, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 169 ...  .. annotations: 3
adding alternatives:[Ringed hair disease, Pili annulati, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=169]
processing orphanet number: 85203 ...  .. annotations: 4
adding alternatives:[Acro-pectoral syndrome, ACRP syndrome, Syndactyly - preaxial polydactyly - sternal deformity, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85203]
processing orphanet number: 48652 ...  .. annotations: 35
adding alternatives:[Monosomy 22q13, 22q13 deletion, Phelan-McDermid syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=48652]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 85202 ...  .. annotations: 26
adding alternatives:[Keutel syndrome, Pulmonic stenosis - brachytelephalangism - calcification of cartilages, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85202]
processing orphanet number: 1827 ...  .. annotations: 6
adding alternatives:[Acromelic frontonasal dysplasia, Toriello syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1827]
processing orphanet number: 85201 ...  .. annotations: 35
adding alternatives:[Genitopatellar syndrome, Absent patellae - scrotal hypoplasia - renal anomalies - facial dysmorphism - intellectual disability, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85201]
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1826 ...  .. annotations: 33
adding alternatives:[Frontometaphyseal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1826]
processing orphanet number: 1825 ...  .. annotations: 26
processing orphanet number: 1824 ...  .. annotations: 20
adding alternatives:[Lowry-Wood syndrome, Epiphyseal dysplasia - microcephaly - nystagmus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1824]
processing orphanet number: 63440 ...  .. annotations: 5
processing orphanet number: 63442 ...  .. annotations: 9
adding alternatives:[Angel-shaped phalango-epiphyseal dysplasia, ASPED, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=63442]
processing orphanet number: 73246 ...  .. annotations: 26
processing orphanet number: 99874 ...  .. annotations: 6
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 63446 ...  .. annotations: 20
adding alternatives:[Acrocapitofemoral dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=63446]
processing orphanet number: 99873 ...  .. annotations: 7
processing orphanet number: 170 ...  .. annotations: 14
processing orphanet number: 99876 ...  .. annotations: 10
adding alternatives:[Ehlers-Danlos syndrome, arthrochalasic type, EDS VII, Ehlers-Danlos syndrome type 7, Ehlers-Danlos syndrome, arthrochalasia type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1899, Ehlers-Danlos syndrome type 7A, EDS VIIA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99875, Ehlers-Danlos syndrome type 7B, EDS VIIB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99876]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23150
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 99875 ...  .. annotations: 7
adding alternatives:[Ehlers-Danlos syndrome, arthrochalasic type, EDS VII, Ehlers-Danlos syndrome type 7, Ehlers-Danlos syndrome, arthrochalasia type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1899, Ehlers-Danlos syndrome type 7A, EDS VIIA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99875, Ehlers-Danlos syndrome type 7B, EDS VIIB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99876]
processing orphanet number: 172 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 173 ...  .. annotations: 14
processing orphanet number: 174 ...  .. annotations: 17
adding alternatives:[Metaphyseal chondrodysplasia, Schmid type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=174]
  ... no hpo-term mapping for orphanet annotation: 45930
  ... no hpo-term mapping for orphanet annotation: 16000
processing orphanet number: 99872 ...  .. annotations: 22
processing orphanet number: 175 ...  .. annotations: 84
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=175]
  ... no hpo-term mapping for orphanet annotation: 20340
  ... no hpo-term mapping for orphanet annotation: 45930
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 99871 ...  .. annotations: 28
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 176 ...  .. annotations: 75
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 139471 ...  .. annotations: 23
adding alternatives:[Microphthalmia with brain and digit anomalies, Bakrania-Ragge syndrome, MCOPS6, Syndromic microphthalmia type 6, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139471]
processing orphanet number: 1832 ...  .. annotations: 20
adding alternatives:[Lethal osteosclerotic bone dysplasia, Raine syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1832]
processing orphanet number: 177 ...  .. annotations: 20
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1830 ...  .. annotations: 20
adding alternatives:[Schimke immuno-osseous dysplasia, Schimke syndrome, Spondyloepiphyseal dysplasia - nephrotic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1830]
processing orphanet number: 1839 ...  .. annotations: 18
adding alternatives:[Hereditary mucoepithelial dysplasia, Urban-Schosser-Spohn syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1839]
processing orphanet number: 139474 ...  .. annotations: 17
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=636, 17q11.2 microduplication syndrome, Dup(17)(q11.2), Grisart-Destrée syndrome, Trisomy 17q11.2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139474, 17q11 microdeletion syndrome, Del(17)(q11), Monosomy 17q11, NF1 microdeletion syndrome, Neurofibromatosis type 1 microdeletion syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=97685]
processing orphanet number: 1837 ...  .. annotations: 16
adding alternatives:[Ulna metaphyseal dysplasia syndrome, Rosenberg-Lohr syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1837]
processing orphanet number: 1836 ...  .. annotations: 15
processing orphanet number: 1834 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 99867 ...  .. annotations: 35
adding alternatives:[Thymoma, Primary thymic epithelial neoplasm, Primary thymic epithelial tumor, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99867]
  ... no hpo-term mapping for orphanet annotation: 32600
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 63455 ...  .. annotations: 2
processing orphanet number: 99868 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 33400
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 180 ...  .. annotations: 8
adding alternatives:[Choroideremia, CHM, Tapetochoroidal dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=180]
processing orphanet number: 181 ...  .. annotations: 14
adding alternatives:[X-linked hypohidrotic ectodermal dysplasia, Christ-Siemens-Touraine syndrome, X-linked anhidrotic ectodermal dysplasia, XHED, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=181, Hypohidrotic ectodermal dysplasia, Anhidrotic ectodermal dysplasia, HED, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238468]
processing orphanet number: 183 ...  .. annotations: 55
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 38160
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 27660
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 184 ...  .. annotations: 13
adding alternatives:[Cherubism, CRBM, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=184]
  ... no hpo-term mapping for orphanet annotation: 3560
processing orphanet number: 221016 ...  .. annotations: 25
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 188 ...  .. annotations: 26
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 189 ...  .. annotations: 26
adding alternatives:[Hidrotic ectodermal dysplasia, Clouston syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=189]
processing orphanet number: 1842 ...  .. annotations: 42
adding alternatives:[Bone dysplasia, lethal Holmgren type, Autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1842]
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1849 ...  .. annotations: 2
adding alternatives:[Infundibulopelvic stenosis - multicystic kidney, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1849]
processing orphanet number: 1848 ...  .. annotations: 18
processing orphanet number: 324723 ...  .. annotations: 3
adding alternatives:[ABetaA21G amyloidosis, ABetaA21G-related amyloidosis, Beta amyloidosis, Flemish type, HCHWA, Flemish type, Hereditary cerebral hemorrhage with amyloidosis, Flemish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324718, ABeta amyloidosis, Italian type, ABetaE22K amyloidosis, HCHWA, Italian type, Hereditary cerebral hemorrhage with amyloidosis, Italian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324713, ABeta amyloidosis, Arctic type, ABetaE22G amyloidosis, HCHWA, Arctic type, Hereditary cerebral hemorrhage with amyloidosis, Arctic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324723, ABeta amyloidosis, Iowa type, ABetaD23N amyloidosis, HCHWA, Iowa type, Hereditary cerebral hemorrhage with amyloidosis, Iowa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324708, ABetaL34V amyloidosis, ABetaL34V-related amyloidosis, Beta amyloidosis, Piedmont type, HCHWA, Piedmont type, Hereditary cerebral hemorrhage with amyloidosis, Piedmont type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324703, Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ABeta amyloidosis, Dutch type, ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, Hereditary cerebral hemorrhage with amyloidosis, Dutch type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100006]
processing orphanet number: 190 ...  .. annotations: 9
NO OMIMENTRY FOR OMIM-ID 300216 creating NEW one
processing orphanet number: 191 ...  .. annotations: 61
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 24000
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 192 ...  .. annotations: 68
adding alternatives:[Coffin-Lowry syndrome, CLS, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=192]
  ... no hpo-term mapping for orphanet annotation: 20380
  ... no hpo-term mapping for orphanet annotation: 3600
processing orphanet number: 193 ...  .. annotations: 61
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=193]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 194 ...  .. annotations: 2
processing orphanet number: 79373 ...  .. annotations: 48
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 93672 ...  .. annotations: 44
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 33400
processing orphanet number: 195 ...  .. annotations: 21
adding alternatives:[Cat-eye syndrome, Chromosome 22 inversion/duplication, Ocular coloboma - imperforate anus, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=195]
processing orphanet number: 1855 ...  .. annotations: 12
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1855]
processing orphanet number: 198 ...  .. annotations: 49
adding alternatives:[Occipital horn syndrome, EDS IX, Ehlers-Danlos syndrome type IX, Ehlers-Danlos syndrome, type 9, X-linked cutis laxa, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=198]
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 199 ...  .. annotations: 95
  ... no hpo-term mapping for orphanet annotation: 27240
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2701 ...  .. annotations: 30
adding alternatives:[Noonan syndrome-like disorder with loose anagen hair, NS/LAH, Tosti syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2701]
processing orphanet number: 314911 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 27240
processing orphanet number: 1852 ...  .. annotations: 6
adding alternatives:[X-linked retinal dysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1852]
processing orphanet number: 1850 ...  .. annotations: 9
processing orphanet number: 314918 ...  .. annotations: 5
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 2709 ...  .. annotations: 8
adding alternatives:[Oculodental syndrome, Rutherfurd type, Gingival hypertrophy-corneal dystrophy, Rutherfurd syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2709]
processing orphanet number: 2707 ...  .. annotations: 31
adding alternatives:[Oculocerebrofacial syndrome, Kaufman type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2707]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1858 ...  .. annotations: 15
adding alternatives:[Skeletal dysplasia - epilepsy - short stature, Gurrieri-Sammito-Bellussi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1858]
processing orphanet number: 2705 ...  .. annotations: 5
processing orphanet number: 2704 ...  .. annotations: 12
  ... no hpo-term mapping for orphanet annotation: 54210
processing orphanet number: 2703 ...  .. annotations: 6
processing orphanet number: 1856 ...  .. annotations: 13
adding alternatives:[Spondyloperipheral dysplasia - short ulna, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1856]
processing orphanet number: 70567 ...  .. annotations: 9
adding alternatives:[Cholangiocarcinoma, Bile duct cancer, CCA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=70567]
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 90154 ...  .. annotations: 25
adding alternatives:[Mandibuloacral dysplasia, MAD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2457, Mandibuloacral dysplasia with type B lipodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90154]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 90153 ...  .. annotations: 28
adding alternatives:[Mandibuloacral dysplasia, MAD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2457, Mandibuloacral dysplasia with type A lipodystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90153]
  ... no hpo-term mapping for orphanet annotation: 46000
processing orphanet number: 324713 ...  .. annotations: 7
adding alternatives:[ABetaA21G amyloidosis, ABetaA21G-related amyloidosis, Beta amyloidosis, Flemish type, HCHWA, Flemish type, Hereditary cerebral hemorrhage with amyloidosis, Flemish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324718, ABeta amyloidosis, Italian type, ABetaE22K amyloidosis, HCHWA, Italian type, Hereditary cerebral hemorrhage with amyloidosis, Italian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324713, ABeta amyloidosis, Arctic type, ABetaE22G amyloidosis, HCHWA, Arctic type, Hereditary cerebral hemorrhage with amyloidosis, Arctic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324723, ABeta amyloidosis, Iowa type, ABetaD23N amyloidosis, HCHWA, Iowa type, Hereditary cerebral hemorrhage with amyloidosis, Iowa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324708, ABetaL34V amyloidosis, ABetaL34V-related amyloidosis, Beta amyloidosis, Piedmont type, HCHWA, Piedmont type, Hereditary cerebral hemorrhage with amyloidosis, Piedmont type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324703, Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ABeta amyloidosis, Dutch type, ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, Hereditary cerebral hemorrhage with amyloidosis, Dutch type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100006]
processing orphanet number: 79361 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 79364 ...  .. annotations: 7
processing orphanet number: 2713 ...  .. annotations: 19
adding alternatives:[Oculoosteocutaneous syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2713]
  ... no hpo-term mapping for orphanet annotation: 3600
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1865 ...  .. annotations: 18
adding alternatives:[Dyssegmental dysplasia, Silverman-Handmaker type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1865]
processing orphanet number: 2712 ...  .. annotations: 39
adding alternatives:[Microphthalmia, Lenz type, Lenz microphthalmia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=568, Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2712]
processing orphanet number: 79365 ...  .. annotations: 13
processing orphanet number: 2710 ...  .. annotations: 86
processing orphanet number: 1863 ...  .. annotations: 4
processing orphanet number: 1861 ...  .. annotations: 14
adding alternatives:[Thoracic dysplasia-hydrocephalus syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1861]
processing orphanet number: 1860 ...  .. annotations: 42
adding alternatives:[Thanatophoric dysplasia, TD, Thanatophoric dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2655, Thanatophoric dysplasia type 1, TD1, Thanatophoric dwarfism type 1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1860]
  ... no hpo-term mapping for orphanet annotation: 23150
processing orphanet number: 2719 ...  .. annotations: 44
adding alternatives:[Oculocerebral hypopigmentation syndrome, Cross type, Cross syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2719]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2718 ...  .. annotations: 14
adding alternatives:[Oculotrichodysplasia, Cecato de Lima-Pinheiro syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2718]
processing orphanet number: 2717 ...  .. annotations: 10
adding alternatives:[Oculotrichoanal syndrome, MOTA syndrome, Manitoba oculotrichoanal syndrome, Marles syndrome, Marles-Greenberg-Persaud syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2717]
  ... no hpo-term mapping for orphanet annotation: 24760
processing orphanet number: 2716 ...  .. annotations: 20
processing orphanet number: 2715 ...  .. annotations: 29
adding alternatives:[Oculorenocerebellar syndrome, Hunter-Jurenka-Thompson syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2715]
processing orphanet number: 1867 ...  .. annotations: 12
adding alternatives:[Bullous dystrophy, macular type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1867]
processing orphanet number: 2714 ...  .. annotations: 30
adding alternatives:[Oculo-palato-cerebral syndrome, Oculo-palato-cerebral dwarfism, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2714]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 324703 ...  .. annotations: 13
adding alternatives:[ABetaA21G amyloidosis, ABetaA21G-related amyloidosis, Beta amyloidosis, Flemish type, HCHWA, Flemish type, Hereditary cerebral hemorrhage with amyloidosis, Flemish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324718, ABeta amyloidosis, Italian type, ABetaE22K amyloidosis, HCHWA, Italian type, Hereditary cerebral hemorrhage with amyloidosis, Italian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324713, ABeta amyloidosis, Arctic type, ABetaE22G amyloidosis, HCHWA, Arctic type, Hereditary cerebral hemorrhage with amyloidosis, Arctic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324723, ABeta amyloidosis, Iowa type, ABetaD23N amyloidosis, HCHWA, Iowa type, Hereditary cerebral hemorrhage with amyloidosis, Iowa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324708, ABetaL34V amyloidosis, ABetaL34V-related amyloidosis, Beta amyloidosis, Piedmont type, HCHWA, Piedmont type, Hereditary cerebral hemorrhage with amyloidosis, Piedmont type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324703, Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ABeta amyloidosis, Dutch type, ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, Hereditary cerebral hemorrhage with amyloidosis, Dutch type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100006]
  ... no hpo-term mapping for orphanet annotation: 43190
  ... no hpo-term mapping for orphanet annotation: 43400
processing orphanet number: 1880 ...  .. annotations: 19
adding alternatives:[Ebstein malformation, Ebstein anomaly of the tricuspid valve, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1880]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 35390
processing orphanet number: 324708 ...  .. annotations: 10
adding alternatives:[ABetaA21G amyloidosis, ABetaA21G-related amyloidosis, Beta amyloidosis, Flemish type, HCHWA, Flemish type, Hereditary cerebral hemorrhage with amyloidosis, Flemish type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324718, ABeta amyloidosis, Italian type, ABetaE22K amyloidosis, HCHWA, Italian type, Hereditary cerebral hemorrhage with amyloidosis, Italian type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324713, ABeta amyloidosis, Arctic type, ABetaE22G amyloidosis, HCHWA, Arctic type, Hereditary cerebral hemorrhage with amyloidosis, Arctic type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324723, ABeta amyloidosis, Iowa type, ABetaD23N amyloidosis, HCHWA, Iowa type, Hereditary cerebral hemorrhage with amyloidosis, Iowa type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324708, ABetaL34V amyloidosis, ABetaL34V-related amyloidosis, Beta amyloidosis, Piedmont type, HCHWA, Piedmont type, Hereditary cerebral hemorrhage with amyloidosis, Piedmont type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=324703, Hereditary cerebral hemorrhage with amyloidosis, HCHWA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=85458, ABeta amyloidosis, Dutch type, ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, Hereditary cerebral hemorrhage with amyloidosis, Dutch type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100006]
processing orphanet number: 86918 ...  .. annotations: 4
processing orphanet number: 79395 ...  .. annotations: 6
adding alternatives:[Keratoderma hereditarium mutilans with ichthyosis, Camisa disease, Keratoderma - ichthyosiform dermatosis - elevated beta-glucuronidase, Loricrin keratoderma, Vohwinkel syndrome - ichthyosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79395]
  ... no hpo-term mapping for orphanet annotation: 43190
processing orphanet number: 86919 ...  .. annotations: 9
adding alternatives:[Keratosis palmaris et plantaris - clinodactyly, Palmoplantar keratoderma - clinodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86919]
processing orphanet number: 79394 ...  .. annotations: 14
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 79397 ...  .. annotations: 10
adding alternatives:[Epidermolysis bullosa simplex with mottled pigmentation, EBS-MP, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79397]
processing orphanet number: 79396 ...  .. annotations: 18
adding alternatives:[Epidermolysis bullosa simplex, Dowling-Meara type, Epidermolysis bullosa simplex, herpetiformis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79396]
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1877 ...  .. annotations: 13
processing orphanet number: 2724 ...  .. annotations: 5
adding alternatives:[Odontomatosis - aortae esophagus stenosis, Boder syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2724]
processing orphanet number: 79399 ...  .. annotations: 17
adding alternatives:[Generalized epidermolysis bullosa simplex, non-Dowling-Meara type, Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex, Köbner type, Generalized EBS, non-Dowling-Meara type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79399]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1876 ...  .. annotations: 10
adding alternatives:[Oculogastrointestinal muscular dystrophy, Visceral myopathy - familial external ophthalmoplegia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1876]
processing orphanet number: 2723 ...  .. annotations: 30
adding alternatives:[Odontotrichomelic syndrome, Freire-Maia syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2723]
  ... no hpo-term mapping for orphanet annotation: 18480
processing orphanet number: 59305 ...  .. annotations: 9
processing orphanet number: 1875 ...  .. annotations: 15
adding alternatives:[Congenital muscular dystrophy - infantile cataract - hypogonadism, Bassoe syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1875]
processing orphanet number: 2722 ...  .. annotations: 12
processing orphanet number: 86923 ...  .. annotations: 5
adding alternatives:[Hereditary palmoplantar keratoderma, Gamborg-Nielsen type, Hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type, PPK, Gamborg-Nielsen type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86923]
processing orphanet number: 2721 ...  .. annotations: 23
adding alternatives:[Odonto-onycho-dermal dysplasia, OODD, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2721]
processing orphanet number: 1873 ...  .. annotations: 9
adding alternatives:[Jalili syndrome, Cone rod dystrophy - amelogenesis imperfecta, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1873]
processing orphanet number: 2720 ...  .. annotations: 25
adding alternatives:[Oculocerebral hypopigmentation syndrome, Preus type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2720]
processing orphanet number: 1872 ...  .. annotations: 7
processing orphanet number: 1871 ...  .. annotations: 6
processing orphanet number: 59303 ...  .. annotations: 12
adding alternatives:[Ichthyosis - hypotrichosis - sclerosing cholangitis, IHSC, NISCH syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=59303]
processing orphanet number: 2729 ...  .. annotations: 38
NO OMIMENTRY FOR OMIM-ID 604916 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2728 ...  .. annotations: 48
adding alternatives:[Blepharophimosis-intellectual disability syndrome, Ohdo type, BMRS, Ohdo type, Blepharophimosis syndrome, Ohdo type, Ohdo syndrome, Ohdo-Madokoro-Sonoda syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2728]
processing orphanet number: 1879 ...  .. annotations: 6
processing orphanet number: 1878 ...  .. annotations: 7
adding alternatives:[Autosomal recessive limb-girdle muscular dystrophy type 2H, LGMD2H, Limb-girdle muscular dystrophy due to TRIM32 deficiency, Sarcotubular myopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1878]
processing orphanet number: 2725 ...  .. annotations: 24
NO OMIMENTRY FOR OMIM-ID 609465 creating NEW one
processing orphanet number: 1891 ...  .. annotations: 10
adding alternatives:[Intellectual disability - spasticity - ectrodactyly, Jancar syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1891]
processing orphanet number: 86914 ...  .. annotations: 2
adding alternatives:[Lymphedema - cerebral arteriovenous anomaly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=86914]
processing orphanet number: 2733 ...  .. annotations: 6
processing orphanet number: 1885 ...  .. annotations: 15
processing orphanet number: 2732 ...  .. annotations: 14
processing orphanet number: 2731 ...  .. annotations: 7
adding alternatives:[Taurodontia - absent teeth - sparse hair, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2731]
processing orphanet number: 1884 ...  .. annotations: 10
processing orphanet number: 1883 ...  .. annotations: 13
adding alternatives:[Ectodermal dysplasia-sensorineural deafness syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1883]
processing orphanet number: 2730 ...  .. annotations: 3
adding alternatives:[Postaxial tetramelic oligodactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2730]
processing orphanet number: 1882 ...  .. annotations: 14
adding alternatives:[Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia, ANOTHER syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1882]
processing orphanet number: 59315 ...  .. annotations: 15
processing orphanet number: 1409 ...  .. annotations: 20
adding alternatives:[Woolly hair - hypotrichosis - everted lower lip - outstanding ears, Salamon syndrome, Wooly hair - hypotrichosis - everted lower lip - outstanding ears, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1409]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1408 ...  .. annotations: 13
adding alternatives:[Hair defect - photosensitivity - intellectual disability, Calderón-González-Cantu syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1408]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 1406 ...  .. annotations: 16
processing orphanet number: 2736 ...  .. annotations: 7
adding alternatives:[Lethal omphalocele-cleft palate syndrome, Czeizel syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2736]
processing orphanet number: 69127 ...  .. annotations: 19
processing orphanet number: 69126 ...  .. annotations: 18
adding alternatives:[Pyogenic arthritis - pyoderma gangrenosum - acne, FRA, Familial recurrent arthritis, PAPA syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69126]
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
processing orphanet number: 70592 ...  .. annotations: 3
adding alternatives:[Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency, IRAK4 deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=70592]
processing orphanet number: 2746 ...  .. annotations: 27
adding alternatives:[Opsismodysplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2746]
processing orphanet number: 1415 ...  .. annotations: 8
adding alternatives:[Cholestasis - pigmentary retinopathy - cleft palate, Hardikar syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1415]
  ... no hpo-term mapping for orphanet annotation: 26460
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1899 ...  .. annotations: 19
adding alternatives:[Ehlers-Danlos syndrome, arthrochalasic type, EDS VII, Ehlers-Danlos syndrome type 7, Ehlers-Danlos syndrome, arthrochalasia type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1899, Ehlers-Danlos syndrome type 7A, EDS VIIA, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99875, Ehlers-Danlos syndrome type 7B, EDS VIIB, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99876]
  ... no hpo-term mapping for orphanet annotation: 23000
processing orphanet number: 1414 ...  .. annotations: 20
adding alternatives:[Cholestasis-lymphedema syndrome, Aagenaes syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1414]
  ... no hpo-term mapping for orphanet annotation: 27420
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 2745 ...  .. annotations: 22
processing orphanet number: 2744 ...  .. annotations: 9
adding alternatives:[Horizontal gaze palsy with progressive scoliosis, HGPPS, Progressive external ophthalmoplegia and scoliosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2744]
processing orphanet number: 1897 ...  .. annotations: 16
adding alternatives:[EEM syndrome, Ectodermal dysplasia - ectrodactyly - macular dystrophy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1897]
processing orphanet number: 1412 ...  .. annotations: 4
processing orphanet number: 1896 ...  .. annotations: 50
processing orphanet number: 2743 ...  .. annotations: 10
adding alternatives:[Ophthalmoplegia - intellectual disability - lingua scrotalis, Levic-Stefanovic-Nikolic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2743]
processing orphanet number: 1895 ...  .. annotations: 28
adding alternatives:[Edinburgh malformation syndrome, Typus Edinburgensis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1895]
  ... no hpo-term mapping for orphanet annotation: 24400
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2742 ...  .. annotations: 4
processing orphanet number: 1410 ...  .. annotations: 7
adding alternatives:[Uncombable hair syndrome, Pili trianguli et canaliculi, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1410]
  ... no hpo-term mapping for orphanet annotation: 24000
processing orphanet number: 2741 ...  .. annotations: 17
adding alternatives:[Ophthalmomandibulomelic dysplasia, OMM syndrome, Pillay syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2741]
processing orphanet number: 1894 ...  .. annotations: 6
processing orphanet number: 1892 ...  .. annotations: 8
adding alternatives:[Ectrodactyly - polydactyly, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1892]
processing orphanet number: 2749 ...  .. annotations: 6
processing orphanet number: 1416 ...  .. annotations: 13
processing orphanet number: 238750 ...  .. annotations: 42
adding alternatives:[4q21 microdeletion syndrome, Del(4)(q21), Monosomy 4q21, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=238750]
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2760 ...  .. annotations: 9
adding alternatives:[OSLAM syndrome, Osteosarcoma - limb anomalies - erythroid macrocytosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2760]
processing orphanet number: 1426 ...  .. annotations: 16
adding alternatives:[Greenberg dysplasia, Hydrops - ectopic calcification - motheaten, Skeletal dysplasia, Greenberg type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1426]
processing orphanet number: 1425 ...  .. annotations: 28
processing orphanet number: 2756 ...  .. annotations: 16
adding alternatives:[Orofaciodigital syndrome type 10, Figuera syndrome, OFD10, Oral-facial-digital syndrome type 10, Orofaciodigital syndrome with fibular aplasia, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2756]
processing orphanet number: 2755 ...  .. annotations: 35
adding alternatives:[Orofaciodigital syndrome type 8, OFD8, Oral-facial-digital syndrome type 8, Oral-facial-digital syndrome, Edwards type, Orofaciodigital syndrome, Edwards type, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2755]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 2754 ...  .. annotations: 36
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1423 ...  .. annotations: 26
processing orphanet number: 1422 ...  .. annotations: 23
adding alternatives:[Chondrodysplasia - disorder of sex development, Chondrodysplasia - pseudohermaphroditism, Nivelon-Nivelon-Mabille syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1422]
processing orphanet number: 2753 ...  .. annotations: 46
adding alternatives:[Orofaciodigital syndrome type 4, Baraitser-Burn syndrome, OFD4, Oral-facial-digital syndrome type 4, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2753]
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2752 ...  .. annotations: 27
adding alternatives:[Orofaciodigital syndrome type 3, OFD3, Oral-facial-digital syndrome type 3, Sugarman syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2752]
  ... no hpo-term mapping for orphanet annotation: 10420
processing orphanet number: 1420 ...  .. annotations: 26
processing orphanet number: 2751 ...  .. annotations: 32
adding alternatives:[Orofaciodigital syndrome type 2, Mohr syndrome, OFD2, Oral-facial-digital syndrome type 2, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2751]
processing orphanet number: 2750 ...  .. annotations: 67
adding alternatives:[Moved to, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2750]
  ... no hpo-term mapping for orphanet annotation: 10420
  ... no hpo-term mapping for orphanet annotation: 43260
processing orphanet number: 1429 ...  .. annotations: 2
processing orphanet number: 2759 ...  .. annotations: 20
processing orphanet number: 1427 ...  .. annotations: 19
adding alternatives:[Otospondylomegaepiphyseal dysplasia, OSMED, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1427]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 93258 ...  .. annotations: 20
processing orphanet number: 93256 ...  .. annotations: 29
adding alternatives:[Fragile X-associated tremor/ataxia syndrome, FXTAS syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=93256]
  ... no hpo-term mapping for orphanet annotation: 52660
  ... no hpo-term mapping for orphanet annotation: 43180
processing orphanet number: 93259 ...  .. annotations: 34
processing orphanet number: 2771 ...  .. annotations: 15
processing orphanet number: 2770 ...  .. annotations: 28
adding alternatives:[Nasu-Hakola disease, NHD, PLO-SL, PLOSL, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2770]
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 98941 ...  .. annotations: 6
processing orphanet number: 1437 ...  .. annotations: 13
  ... no hpo-term mapping for orphanet annotation: 24760
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 2768 ...  .. annotations: 2
processing orphanet number: 1436 ...  .. annotations: 8
adding alternatives:[Skeletal dysplasia - intellectual disability, Christian syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1436]
processing orphanet number: 2767 ...  .. annotations: 4
adding alternatives:[Carpotarsal osteochondromatosis, Maroteaux-Le Merrer-Bensahel syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2767]
processing orphanet number: 1435 ...  .. annotations: 5
adding alternatives:[Choroideremia - deafness - obesity, Ayazi syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1435]
processing orphanet number: 1434 ...  .. annotations: 10
processing orphanet number: 1433 ...  .. annotations: 11
processing orphanet number: 2763 ...  .. annotations: 63
adding alternatives:[Osteocraniostenosis, Gracile bone dysplasia, Osteocraniosplenic syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2763]
processing orphanet number: 281127 ...  .. annotations: 1
processing orphanet number: 2762 ...  .. annotations: 14
adding alternatives:[Progressive osseous heteroplasia, Familial ectopic ossification, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2762]
  ... no hpo-term mapping for orphanet annotation: 45690
processing orphanet number: 281122 ...  .. annotations: 3
processing orphanet number: 1438 ...  .. annotations: 25
processing orphanet number: 2769 ...  .. annotations: 25
NO OMIMENTRY FOR OMIM-ID 259250 creating NEW one
processing orphanet number: 95429 ...  .. annotations: 10
  ... no hpo-term mapping for orphanet annotation: 23000
  ... no hpo-term mapping for orphanet annotation: 23600
processing orphanet number: 46059 ...  .. annotations: 43
adding alternatives:[Lathosterolosis, Sterol C5-desaturase deficiency, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46059]
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 1451 ...  .. annotations: 46
NO OMIMENTRY FOR OMIM-ID 607115 creating NEW one
  ... no hpo-term mapping for orphanet annotation: 23480
  ... no hpo-term mapping for orphanet annotation: 54350
  ... no hpo-term mapping for orphanet annotation: 54770
  ... no hpo-term mapping for orphanet annotation: 45690
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 226307 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1450 ...  .. annotations: 14
processing orphanet number: 2781 ...  .. annotations: 48
  ... no hpo-term mapping for orphanet annotation: 16000
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 48080
processing orphanet number: 2780 ...  .. annotations: 32
adding alternatives:[Osteopathia striata - cranial sclerosis, Hyperostosis generalisata with striations, Robinow-Unger syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2780]
processing orphanet number: 1448 ...  .. annotations: 11
processing orphanet number: 2779 ...  .. annotations: 8
adding alternatives:[Osteopathia striata - pigmentary dermopathy - white forelock, Whyte-Murphy syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2779]
processing orphanet number: 226310 ...  .. annotations: 17
  ... no hpo-term mapping for orphanet annotation: 53450
  ... no hpo-term mapping for orphanet annotation: 54350
processing orphanet number: 1447 ...  .. annotations: 4
processing orphanet number: 2777 ...  .. annotations: 7
adding alternatives:[Osteomesopyknosis, Axial osteosclerosis, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2777]
processing orphanet number: 2776 ...  .. annotations: 11
adding alternatives:[Autosomal recessive distal osteolysis syndrome, Distal osteolysis - short stature - intellectual disability, Petit-Fryns syndrome, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2776]
processing orphanet number: 2774 ...  .. annotations: 21
adding alternatives:[Multicentric carpo-tarsal osteolysis with or without nephropathy, Idiopathic multicentric osteolysis with or without nephropathy, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2774]
processing orphanet number: 36258 ...  .. annotations: 12
adding alternatives:[Buerger disease, Thromboangiitis obliterans, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=36258]
  ... no hpo-term mapping for orphanet annotation: 35390
  ... no hpo-term mapping for orphanet annotation: 43400
  ... no hpo-term mapping for orphanet annotation: 35750
processing orphanet number: 2773 ...  .. annotations: 6
processing orphanet number: 2772 ...  .. annotations: 22
adding alternatives:[Congenital osteogenesis imperfecta - microcephaly - cataracts, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2772]
processing orphanet number: 238769 ...  .. annotations: 31
  ... no hpo-term mapping for orphanet annotation: 52480
  ... no hpo-term mapping for orphanet annotation: 53450
processing orphanet number: 230800 ...  .. annotations: 12
processing orphanet number: 306498 ...  .. annotations: 19
  ... no hpo-term mapping for orphanet annotation: 10420
done parsing and merging: writing annotations to file /var/lib/jenkins/jobs/hpo.annotations/workspace/misc/./phenotype_annotation.tab
done.
cat phenotype_annotation.tab negative_phenotype_annotation.tab | awk -F'\t' '{print $14}'  | sort | uniq -c | sort -nr > curator-statistics.tab
echo "2016-01-13 13:18" > data_version.txt
make: Leaving directory '/var/lib/jenkins/jobs/hpo.annotations/workspace/misc'
Archiving artifacts
Sending e-mails to: sebastian.koehler@charite.de
Finished: SUCCESS