DISEASES

Disease-gene associations mined from literature

Human genes for cerebellar ataxia type 41

Cerebellar ataxia type 41 [DOID:0111744]

An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in TRPC3 on chromosome 4q27.

Synonyms:  cerebellar ataxia type 41,  DOID:0111744,  SCA41