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Summary Literature (0)
MIM:601869 - DEAFNESS, AUTOSOMAL RECESSIVE 15; DFNB15

Xenbase Genes: gipc3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011160 - autosomal recessive nonsyndromic hearing loss 15
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110470 - autosomal recessive nonsyndromic deafness 15