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Autosomal dominant nonsyndromic hearing loss 40

MONDO:0014603

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

Also known as: autosomal dominant nonsyndromic hearing loss 40, CRYM autosomal dominant nonsyndromic deafness, DFNA40, autosomal dominant deafness 40, autosomal dominant nonsyndromic deafness 40, autosomal dominant nonsyndromic deafness caused by mutation in CRYM, autosomal dominant nonsyndromic deafness type 40, deafness, autosomal dominant 40

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 40 itself.

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