SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12

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Summary

Literature (0)

MIM:614322 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12

Xenbase Genes: wwox

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013687 - pericranium

MONDO:0013687 - pericranium

Disease Ontology (DO):

DOID:0080060 - autosomal recessive spinocerebellar ataxia 12

DOID:0080060 - autosomal recessive spinocerebellar ataxia 12