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Autosomal dominant nonsyndromic hearing loss 25

MONDO:0011568

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SLC17A8 gene.

Also known as: DFNA25, SLC17A8 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 25, autosomal dominant nonsyndromic deafness 25, autosomal dominant nonsyndromic deafness caused by mutation in SLC17A8, autosomal dominant nonsyndromic deafness type 25, deafness, autosomal dominant 25, deafness, autosomal dominant type 25

60 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hearing loss disorder (254) Nervous system disorder (217) Hereditary disease (172) Perceptual disorders (21) Hearing disorder (19) Human disease (14) Hereditary neurological disease (5) Nonsyndromic genetic hearing loss (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 21 Not yet recruiting 13 Not yet finished but already full! 8 Completed 17 Terminated 1
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