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Summary Literature (0)
OMIM:613916 - DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89


Xenbase Genes: kars1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110534 - autosomal recessive nonsyndromic deafness 89