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Summary Literature (0)
MIM:616204 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18; SCAR18

Xenbase Genes: grid2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014530 - autosomal recessive spinocerebellar ataxia 18
MONDO:0018189 - autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome

Disease Ontology (DO):
DOID:0080042 - autosomal recessive spinocerebellar ataxia 18