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Summary Literature (0)
DOID:0112232 - lissencephaly 3

Disease Ontology Definition: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: LIS3

Xenbase Genes : tuba1cl.3, tuba1a


MIM:
MIM:611603 - LISSENCEPHALY 3; LIS3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), lissencephaly (is_a)