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Summary Literature (0)
MIM:602459 - DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15

Xenbase Genes: pou4f3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011226 - autosomal dominant nonsyndromic hearing loss 15
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110546 - autosomal dominant nonsyndromic deafness 15