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Summary Literature (0)
MIM:612674 - POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT; PHARC

Xenbase Genes: abhd12

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012984 - PHARC syndrome

Disease Ontology (DO):
DOID:0080181 - PHARC syndrome