Search Ontology:
Human Disease

complex cortical dysplasia with other brain malformations 2

Term ID
DOID:0090133
Synonyms
  • CDCBM2
Definition
A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the kinesin family member 5C (KIF5C) gene on chromosome 2q23. (3)
References
Ontology
Human Disease   ( DOID:0090133 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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