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DO Term : complex cortical dysplasia with other brain malformations 4 [DOID:0090138] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin gamma 1 gene on chromosome 17q21.

synonyms:
CDCBM4,
OMIM:615412,
615412

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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