3C syndrome
|
(Orphanet:7)
|
Axenfeld anomaly
|
(Orphanet:98978)
|
CAMOS syndrome
|
(Orphanet:83472)
|
IRIDOGONIODYSGENESIS, TYPE 1
|
(OMIM:601631)
|
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
|
(OMIM:606369)
|
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1
|
(OMIM:613155)
|
Noonan syndrome-like disorder with loose anagen hair
|
(Orphanet:2701)
|
Pontocerebellar hypoplasia, type 9
|
(OMIM:615809)
|
SOTOS SYNDROME 1
|
(OMIM:117550)
|
STEVENSON-CAREY SYNDROME
|
(OMIM:611961)
|
Sotos syndrome
|
(Orphanet:821)
|
X-linked intellectual deficit - cerebellar hypoplasia
|
(Orphanet:137831)
|