cerebellar ataxia type 41

Term ID

DOID:0111744

Synonyms

• SCA41

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

References

• OMIM:616410
• ORDO:458798

Ontology

Human Disease   ( DOID:0111744 )