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Summary Literature (0)
MIM:610212 - DEAFNESS, AUTOSOMAL RECESSIVE 66; DFNB66

Xenbase Genes: dcdc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012442 - autosomal recessive nonsyndromic hearing loss 66
MONDO:0019588 - hearing loss, autosomal recessive