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Summary Literature (0)
DOID:0111744 - cerebellar ataxia type 41

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27.

Synonyms: SCA41

Xenbase Genes : trpc3


MIM:
MIM:616410 - SPINOCEREBELLAR ATAXIA 41; SCA41

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

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