DISEASES

Disease-gene associations mined from literature

Human genes for spinocerebellar ataxia type 12

Spinocerebellar ataxia type 12 [DOID:0050962]

An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene.

Synonyms:  spinocerebellar ataxia type 12,  DOID:0050962