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DO Term : complex cortical dysplasia with other brain malformations 9 [DOID:0061138] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A complex cortical dysplasia with other brain malformations characterized by profoundly impaired motor and cognitive development apparent from early infancy that has_material_basis_in homozygous mutation in the CTNNA2 gene on chromosome 2p12.

synonyms:
OMIM:618174,
618174,
CDCBM9

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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