Deafness, Autosomal Dominant 23 (DFNA23)

Alias:

Dfna23

Autosomal Dominant Nonsyndromic Deafness 23

Autosomal Dominant Nonsyndromic Hearing Loss 23

Deafness, Autosomal Dominant, Type 23

Deafness, Autosomal Dominant, 23

Autosomal Dominant Deafness 23

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 23, also known as dfna23, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a and branchiootorenal spectrum disorder. An important gene associated with Deafness, Autosomal Dominant 23 is SIX1 (SIX Homeobox 1). Affiliated tissues include kidney, and related phenotypes are conductive hearing impairment and preauricular pit

Related ID：

MALACARDS：DFN192

OMIM：605192

MESH：D006319