Autosomal dominant nonsyndromic hearing loss 4B

MONDO:0013823

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CEACAM16 gene.

Also known as: CEACAM16 autosomal dominant nonsyndromic deafness, DFNA4B, autosomal dominant deafness 4B, autosomal dominant nonsyndromic deafness 4B, autosomal dominant nonsyndromic deafness caused by mutation in CEACAM16, autosomal dominant nonsyndromic deafness type 4B, deafness, autosomal dominant 4B, deafness, autosomal dominant 4b

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 4B itself.

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