1p36 deletion syndrome
|
(Orphanet:1606)
|
Aicardi syndrome
|
(Orphanet:50)
|
Arnold-Chiari malformation type II
|
(Orphanet:1136)
|
BAND HETEROTOPIA OF BRAIN
|
(OMIM:600348)
|
Bohring-Opitz syndrome
|
(Orphanet:97297)
|
Hydrolethalus
|
(Orphanet:2189)
|
Joubert syndrome 21
|
(OMIM:615636)
|
Joubert syndrome with oculorenal defect
|
(Orphanet:2318)
|
Lissencephaly due to LIS1 mutation
|
(Orphanet:95232)
|
Lissencephaly due to TUBA1A mutation
|
(Orphanet:171680)
|
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
|
(OMIM:210710)
|
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS
|
(OMIM:604317)
|
Microcephalic osteodysplastic primordial dwarfism types 1 and 3
|
(Orphanet:2636)
|
Miller-Dieker syndrome
|
(Orphanet:531)
|
Mowat-Wilson syndrome
|
(Orphanet:2152)
|
Nodular neuronal heterotopia
|
(Orphanet:2149)
|
OPITZ-KAVEGGIA SYNDROME
|
(OMIM:305450)
|
Oculocerebrocutaneous syndrome
|
(Orphanet:1647)
|
PERIVENTRICULAR NODULAR HETEROTOPIA 6
|
(OMIM:615544)
|
Thanatophoric dysplasia type 1
|
(Orphanet:1860)
|
Zellweger syndrome
|
(Orphanet:912)
|