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Summary Literature (0)
MIM:614831 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13

Xenbase Genes: grm1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013905 - autosomal recessive spinocerebellar ataxia 13
MONDO:0018189 - autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome

Disease Ontology (DO):
DOID:0080062 - autosomal recessive spinocerebellar ataxia 13