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Summary Literature (1)
MIM:601338 - CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS

Xenbase Genes: atp1a3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011038 - cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome