Deafness, Autosomal Dominant 20 (DFNA20)

Alias:

Dfna20

Dfna26

Autosomal Dominant Nonsyndromic Deafness 20

Deafness, Autosomal Dominant 20/26

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 20

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 20

Autosomal Dominant Nonsyndromic Hearing Loss 20

Deafness, Autosomal Dominant, Type 20/26

Deafness, Autosomal Dominant, 20

Autosomal Dominant Deafness 20

Deafness Autosomal Dominant 26

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 20, also known as dfna20, is related to baraitser-winter syndrome 2 and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Dominant 20 is ACTG1 (Actin Gamma 1), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include brain and endothelial, and related phenotypes are bilateral sensorineural hearing impairment and progressive sensorineural hearing impairment

Related ID：

MALACARDS：DFN354

OMIM：604717

MESH：D006319