Acro-renal-ocular syndrome
|
(Orphanet:959)
|
Brachydactyly - preaxial hallux varus
|
(Orphanet:1278)
|
Brachydactyly type A1
|
(Orphanet:93388)
|
Brachydactyly type A2
|
(Orphanet:93396)
|
Cleft palate - stapes fixation - oligodontia
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(Orphanet:2010)
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Deafness - genital anomalies - metacarpal and metatarsal synostosis
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(Orphanet:3224)
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Fibrodysplasia ossificans progressiva
|
(Orphanet:337)
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Guttmacher syndrome
|
(Orphanet:2957)
|
Hand-foot-genital syndrome
|
(Orphanet:2438)
|
Hypertrichotic osteochondrodysplasia, Cantu type
|
(Orphanet:1517)
|
Keipert syndrome
|
(Orphanet:2662)
|
Keutel syndrome
|
(Orphanet:85202)
|
MULTIPLE SYNOSTOSES SYNDROME 1
|
(OMIM:186500)
|
Mesoaxial synostotic syndactyly with phalangeal reduction
|
(Orphanet:157801)
|
Mononen-Karnes-Senac syndrome
|
(Orphanet:2565)
|
Multiple synostoses syndrome
|
(Orphanet:3237)
|
OTOFACIOOSSEOUS-GONADAL SYNDROME
|
(OMIM:601976)
|
Oculodentodigital dysplasia
|
(Orphanet:2710)
|
Otopalatodigital syndrome
|
(Orphanet:669)
|
Otopalatodigital syndrome type 1
|
(Orphanet:90650)
|
Otopalatodigital syndrome type 2
|
(Orphanet:90652)
|
Pfeiffer syndrome type 1
|
(Orphanet:93258)
|
Pfeiffer syndrome type 2
|
(Orphanet:93259)
|
Pfeiffer syndrome type 3
|
(Orphanet:93260)
|
SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1
|
(OMIM:119100)
|
Tibial aplasia - ectrodactyly
|
(Orphanet:3329)
|
Wolf-Hirschhorn syndrome
|
(Orphanet:280)
|