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Autosomal recessive nonsyndromic hearing loss 21

MONDO:0011351

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

Also known as: autosomal recessive nonsyndromic hearing loss 21, DFNB21, TECTA autosomal recessive nonsyndromic deafness, autosomal recessive deafness 21, autosomal recessive nonsyndromic deafness 21, autosomal recessive nonsyndromic deafness caused by mutation in TECTA, autosomal recessive nonsyndromic deafness caused by mutation in tecta, autosomal recessive nonsyndromic deafness type 21

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 21 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 21 (0)

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