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DO Term : lissencephaly 3 [DOID:0112232] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A lissencephaly characterized by brain malformations, microcephaly, developmental delay and epilepsy that has_material_basis_in heterozygous mutation in the TUBA1A gene on chromosome 12q13.12.

synonyms:
611603,
OMIM:611603,
MESH:C566908,
LIS3,
ORDO:171680

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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