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Summary Literature (0)
MIM:601386 - DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12

Xenbase Genes: cdh23, atp2b2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011067 - autosomal recessive nonsyndromic hearing loss 12
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110467 - autosomal recessive nonsyndromic deafness 12