Autosomal dominant nonsyndromic hearing loss 69

MONDO:0014738

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

Also known as: DCUA, DFNA69, KITLG autosomal dominant nonsyndromic deafness, autosomal dominant deafness 69, autosomal dominant nonsyndromic deafness 69, autosomal dominant nonsyndromic deafness caused by mutation in KITLG, autosomal dominant nonsyndromic deafness type 69, deafness, autosomal dominant 69

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 69 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 69 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.