Acrorenal syndrome
|
(Orphanet:971)
|
Angio-osteohypertrophic syndrome
|
(Orphanet:2346)
|
Cornelia de Lange syndrome
|
(Orphanet:199)
|
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME
|
(OMIM:246570)
|
Focal dermal hypoplasia
|
(Orphanet:2092)
|
Fuhrmann syndrome
|
(Orphanet:2854)
|
Microgastria - limb reduction defect
|
(Orphanet:2538)
|
Microphthalmia with limb anomalies
|
(Orphanet:1106)
|
Orofaciodigital syndrome type 10
|
(Orphanet:2756)
|
Phocomelia, Schinzel type
|
(Orphanet:2879)
|
Roberts syndrome
|
(Orphanet:3103)
|
Robin sequence - oligodactyly
|
(Orphanet:3104)
|
SPLIT-HAND/FOOT MALFORMATION 6
|
(OMIM:225300)
|
Split hand-split foot malformation
|
(Orphanet:2440)
|
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS
|
(OMIM:276822)
|
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME
|
(OMIM:602418)
|
XK aprosencephaly
|
(Orphanet:3469)
|