Heterotopia

Symptom Information:

Symptom ID: HPO:0002282
Synonyms:
Heterotopias [HPO:0002282]
Heterotopia [OMIM:Heterotopia]
Heterotopias [OMIM:Heterotopias]
Quality:
Cross references:
OMIM: "Heterotopia" [OMIM:Heterotopia]
OMIM: "Heterotopias" [OMIM:Heterotopias]
Is a (Direct Parents):
HPO         Abnormality of neuronal migration
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

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)