autosomal recessive spinocerebellar ataxia 13

Summary

DOID:0080062 - autosomal recessive spinocerebellar ataxia 13

Disease Ontology 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.

Synonyms: SCAR13

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: grm1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013905 - autosomal recessive spinocerebellar ataxia 13

MONDO:0013905 - autosomal recessive spinocerebellar ataxia 13

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive cerebellar ataxia (is_a)