DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive spinocerebellar ataxia 24

Autosomal recessive spinocerebellar ataxia 24 [DOID:0111615]

An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in UBA5 on chromosome 3q22.1.

Synonyms:  autosomal recessive spinocerebellar ataxia 24,  DOID:0111615,  SCAR24