Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616697 - DEAFNESS, AUTOSOMAL DOMINANT 69; DFNA69

Xenbase Genes: kitlg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014738 - autosomal dominant nonsyndromic hearing loss 69
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss