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Disease Ontology Browser
cerebellar ataxia type 41 (DOID:0111744)
Alliance: disease page
Synonyms: SCA41
Alt IDs: OMIM:616410, ORDO:458798
Definition: An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory