Autosomal recessive nonsyndromic hearing loss 6

MONDO:0010965

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

Also known as: autosomal recessive nonsyndromic hearing loss 6, DFNB6, TMIE autosomal recessive nonsyndromic deafness, autosomal recessive deafness 6, autosomal recessive nonsyndromic deafness 6, autosomal recessive nonsyndromic deafness caused by mutation in TMIE, autosomal recessive nonsyndromic deafness type 6, deafness, autosomal recessive 6

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 6 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 6 (0)

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