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Summary Literature (1)
MIM:613865 - DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61

Xenbase Genes: slc26a5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013471 - autosomal recessive nonsyndromic hearing loss 61
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110513 - autosomal recessive nonsyndromic deafness 61