DISEASES

Disease-gene associations mined from literature

Human genes for spinocerebellar ataxia type 25

Spinocerebellar ataxia type 25 [DOID:0050974]

An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21.

Synonyms:  spinocerebellar ataxia type 25,  DOID:0050974