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


Xenbase Genes: ptprq

Human Disease Resource: OMIM

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

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