Acro-pectoral syndrome
|
(Orphanet:85203)
|
Acro-renal-ocular syndrome
|
(Orphanet:959)
|
Acrocallosal syndrome
|
(Orphanet:36)
|
Acrocraniofacial dysostosis
|
(Orphanet:949)
|
Acrofacial dysostosis, Rodriguez type
|
(Orphanet:1788)
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Acropectorovertebral dysplasia
|
(Orphanet:957)
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Arachnodactyly - intellectual deficit - dysmorphism
|
(Orphanet:1130)
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Autosomal recessive deafness-onychodystrophy syndrome
|
(Orphanet:79500)
|
Blackfan-Diamond anemia
|
(Orphanet:124)
|
Bowed tibiae - radial anomalies - osteopenia - fractures
|
(Orphanet:3331)
|
CHARGE syndrome
|
(Orphanet:138)
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Charlie M syndrome
|
(Orphanet:1406)
|
Cooks syndrome
|
(Orphanet:1487)
|
Craniosynostosis, Boston type
|
(Orphanet:1541)
|
DIAMOND-BLACKFAN ANEMIA 1
|
(OMIM:105650)
|
DIAMOND-BLACKFAN ANEMIA 12
|
(OMIM:615550)
|
DIAMOND-BLACKFAN ANEMIA 6
|
(OMIM:612561)
|
DIAMOND-BLACKFAN ANEMIA 7
|
(OMIM:612562)
|
Deafness - onychodystrophy
|
(Orphanet:3231)
|
Deafness - onychodystrophy, autosomal dominant
|
(Orphanet:79499)
|
Fanconi anemia
|
(Orphanet:84)
|
Fetal hydantoin syndrome
|
(Orphanet:1912)
|
Holt-Oram syndrome
|
(Orphanet:392)
|
Hypoplastic tibiae - postaxial polydactyly
|
(Orphanet:3332)
|
IVIC syndrome
|
(Orphanet:2307)
|
Ito hypomelanosis
|
(Orphanet:435)
|
Lacrimo-auriculo-dento-digital syndrome
|
(Orphanet:2363)
|
Laurin-Sandrow syndrome
|
(Orphanet:2378)
|
Lung agenesis - heart defect - thumb anomalies
|
(Orphanet:1120)
|
MMEP syndrome
|
(Orphanet:3434)
|
Multinodular goiter - cystic kidney - polydactyly
|
(Orphanet:2091)
|
Nager syndrome
|
(Orphanet:245)
|
Neurofaciodigitorenal syndrome
|
(Orphanet:2673)
|
Oculoauriculovertebral spectrum with radial defects
|
(Orphanet:2549)
|
Okihiro syndrome
|
(Orphanet:93293)
|
PHAVER syndrome
|
(Orphanet:2876)
|
Pierre Robin syndrome - faciodigital anomaly
|
(Orphanet:2888)
|
Polydactyly of an index finger
|
(Orphanet:93337)
|
Postaxial polydactyly type A
|
(Orphanet:93334)
|
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema
|
(Orphanet:2252)
|
Radial ray hypoplasia - choanal atresia
|
(Orphanet:3026)
|
Rhizomelic syndrome, Urbach type
|
(Orphanet:3098)
|
SPLIT-HAND/FOOT MALFORMATION 4
|
(OMIM:605289)
|
Say-Field-Coldwell syndrome
|
(Orphanet:3133)
|
Short stature - craniofacial anomalies - genital hypoplasia
|
(Orphanet:2994)
|
Split hand-split foot malformation
|
(Orphanet:2440)
|
Syndactyly type 4
|
(Orphanet:93405)
|
TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES
|
(OMIM:190500)
|
TRIPHALANGEAL THUMB, NONOPPOSABLE
|
(OMIM:190600)
|
Thalidomide embryopathy
|
(Orphanet:3312)
|
Thumb deformity - alopecia - pigmentation anomaly
|
(Orphanet:2251)
|
Townes-Brocks syndrome
|
(Orphanet:857)
|
Triphalangeal thumb - polysyndactyly syndrome
|
(Orphanet:2950)
|
Triphalangeal thumbs - brachyectrodactyly
|
(Orphanet:2947)
|
VACTERL/VATER association
|
(Orphanet:887)
|
Van den Ende-Gupta syndrome
|
(Orphanet:2460)
|