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Metadata
ID	DOID:0111744
Name	cerebellar ataxia type 41
Definition	An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27. https://www.ncbi.nlm.nih.gov/pubmed/25477146
Xrefs	OMIM:616410 ORDO:458798
Subsets	DO_rare_slim
Synonyms	SCA41 [EXACT]
Parent Relationships	is_a autosomal dominant cerebellar ataxia