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Summary Literature (0)
MIM:616705 - DEAFNESS, AUTOSOMAL RECESSIVE 97; DFNB97

Xenbase Genes: met

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014739 - autosomal recessive nonsyndromic hearing loss 97
MONDO:0019588 - hearing loss, autosomal recessive