Cure My Disease

Don't miss your cure!

Log in / Sign up

Autosomal dominant nonsyndromic hearing loss 1

MONDO:0007424

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the DIAPH1 gene.

Also known as: Konigsmark syndrome, DFNA1, DIAPH1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 1, autosomal dominant nonsyndromic deafness 1, autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1, autosomal dominant nonsyndromic deafness type 1, deafness, autosomal dominant 1

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

Follow this condition — get notified about new trials

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