DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89

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Summary

Literature (0)

MIM:613916 - DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89

Xenbase Genes: kars1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89
MONDO:0019588 - hearing loss, autosomal recessive

MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89

MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):

DOID:0110534 - autosomal recessive nonsyndromic deafness 89

DOID:0110534 - autosomal recessive nonsyndromic deafness 89