Term Name: autosomal recessive spinocerebellar ataxia 13
Synonyms: SCAR13
Definition: An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.
Ontology: Human Disease [DOID:0080062]   ( DOID:0080062 )

Relationships
is a type of: autosomal recessive cerebellar ataxia