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Summary Literature (0)
MIM:617637 - DEAFNESS, AUTOSOMAL RECESSIVE 106; DFNB106

Xenbase Genes: eps8l2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033198 - hearing loss, autosomal recessive 106

Disease Ontology (DO):
DOID:0080261 - autosomal recessive nonsyndromic deafness 106