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Summary Literature (0)
MIM:607039 - DEAFNESS, AUTOSOMAL RECESSIVE 22; DFNB22

Xenbase Genes: otoa

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011762 - autosomal recessive nonsyndromic hearing loss 22
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110480 - autosomal recessive nonsyndromic deafness 22