Autosomal recessive nonsyndromic hearing loss 89

MONDO:0013489

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the KARS gene.

Also known as: autosomal recessive nonsyndromic hearing loss 89, DFNB89, KARS autosomal recessive nonsyndromic deafness, autosomal recessive deafness 89, autosomal recessive nonsyndromic deafness 89, autosomal recessive nonsyndromic deafness caused by mutation in KARS, autosomal recessive nonsyndromic deafness type 89, deafness, autosomal recessive 89

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 89 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 89 (0)

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