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Summary Literature (0)
DOID:0090131 - complex cortical dysplasia with other brain malformations

Disease Ontology Definition:A brain disease characterized by aberrant neuronal migration and disturbed axonal guidance resulting in variable brain malformations including; polymicrogyria, gyral disorganization, fusion of the basal ganglia, thin corpus callosum, hypoplastic brainstem, and dysplastic cerebellar vermis and behavioral phenotypes including; intellectual disablility, strabismus, axial hypotonia, and spasticity.

Synonyms: CDCBM,

Xenbase Genes : tubb, tubb2b, tubg1, kif2a, kif5c, tubb3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000904 - complex cortical dysplasia with other brain malformations

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

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