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Summary Literature (0)
MIM:610220 - DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59

Xenbase Genes: pjvk

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012445 - autosomal recessive nonsyndromic hearing loss 59
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110511 - autosomal recessive nonsyndromic deafness 59