Deafness, Autosomal Dominant 27 (DFNA27)

Alias:

Dfna27

Autosomal Dominant Nonsyndromic Deafness 27

Autosomal Dominant Nonsyndromic Hearing Loss 27

Deafness, Autosomal Dominant, 27

Autosomal Dominant Deafness 27

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 27, also known as dfna27, is related to deafness, autosomal recessive 2 and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 27 is REST (RE1 Silencing Transcription Factor). Related phenotypes are sensorineural hearing impairment and nervous system

Related ID：

MALACARDS：DFN152

OMIM：612431

MESH：D006319