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Summary Literature (0)
MIM:608224 - DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41

Xenbase Genes: p2rx2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011994 - autosomal dominant nonsyndromic hearing loss 41
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110567 - autosomal dominant nonsyndromic deafness 41