autosomal recessive spinocerebellar ataxia 13

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Summary

Literature (0)

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,

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

OMIM:

MIM:614831 - spinocerebellar ataxia, autosomal recessive 13; scar13

MIM:614831 - spinocerebellar ataxia, autosomal recessive 13; scar13

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

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

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