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Summary Literature (0)
MIM:615974 - DEAFNESS, AUTOSOMAL RECESSIVE 102; DFNB102

Xenbase Genes: eps8

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014428 - autosomal recessive nonsyndromic hearing loss 102
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110463 - autosomal recessive nonsyndromic deafness 102