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:604717 - DEAFNESS, AUTOSOMAL DOMINANT 20; DFNA20

Xenbase Genes: actg1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011480 - autosomal dominant nonsyndromic hearing loss 20
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110550 - autosomal dominant nonsyndromic deafness 20