SuccessConsole Output

Skipping 487 KB.. Full Log
a 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