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Summary Literature (0)
MIM:617663 - DEAFNESS, AUTOSOMAL DOMINANT 73; DFNA73

Xenbase Genes: ptprq

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033260 - hearing loss, autosomal dominant 73

Disease Ontology (DO):
DOID:0080269 - autosomal dominant nonsyndromic deafness 73