autosomal recessive spinocerebellar ataxia 7 (DOID:0080059)
Alliance: disease page
Synonyms: SCAR7
Alt IDs: OMIM:609270
Definition: An autosomal recessive cerebellar ataxia that is characterized by onset of progressive gait difficulties, eye movement abnormalities, and dysarthria in the first or second decade of life and that has_material_basis_in compound heterozygous mutation in the TPP1 gene on chromosome 11p15.