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Summary Literature (0)
MIM:609533 - DEAFNESS, AUTOSOMAL RECESSIVE 23; DFNB23

Xenbase Genes: pcdh15

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012293 - autosomal recessive nonsyndromic hearing loss 23
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110481 - autosomal recessive nonsyndromic deafness 23