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Summary Literature (0)
MIM:614899 - DEAFNESS, AUTOSOMAL RECESSIVE 93; DFNB93

Xenbase Genes: cabp2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013963 - autosomal recessive nonsyndromic hearing loss 93
MONDO:0019588 - hearing loss, autosomal recessive