Home Page
References OMIM Gene GeneReviews HGMD HGNC
last update : 18
Symbol DFNA23
Location 14q21-q22
HGNC id 2795
Name neurosensory deafness 23
Corresponding gene SIX1
Main clinical features non syndromic, prelingual, stable, with hearing ability ranging from normal hearing to mild hearing loss in low frequencies, normal hearing to profound hearing loss in mid-frequencies, and moderate to profound hearing loss in high frequencies
Genetic determination autosomal dominant
Function/system disorder ear
Type disease