Term Name:	autosomal recessive spinocerebellar ataxia 7
Synonyms:	SCAR7
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.
Ontology:	Human Disease [DOID:0080059]   ( DOID:0080059 )