Term Name: autosomal recessive spinocerebellar ataxia 17
Synonyms: SCAR17
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24.
Ontology: Human Disease [DOID:0080064]   ( DOID:0080064 )

Relationships
is a type of: autosomal recessive cerebellar ataxia