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Autosomal recessive nonsyndromic hearing loss 2

MONDO:0010807

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.

Also known as: DFNB2, MYO7A autosomal recessive nonsyndromic deafness, autosomal recessive deafness 2, autosomal recessive nonsyndromic deafness 2, autosomal recessive nonsyndromic deafness caused by mutation in MYO7A, autosomal recessive nonsyndromic deafness type 2, deafness, autosomal recessive 2, deafness, autosomal recessive type 2

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 2 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 2 (0)

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