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Summary Literature (0)
MIM:600316 - DEAFNESS, AUTOSOMAL RECESSIVE 3; DFNB3

Xenbase Genes: myo15a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010860 - autosomal recessive nonsyndromic hearing loss 3
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110488 - autosomal recessive nonsyndromic deafness 3