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Summary Literature (0)
MIM:616795 - SPINOCEREBELLAR ATAXIA 42; SCA42

Xenbase Genes: cacna1g

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014776 - midbrain neuromere

Disease Ontology (DO):
DOID:0111742 - cerebellar ataxia type 42