Deafness, Autosomal Dominant 16 (DFNA16)

Alias:

Autosomal Dominant Nonsyndromic Deafness 16

Dfna16

Autosomal Dominant Nonsyndromic Hearing Loss 16

Autosomal Dominant Deafness 16

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 16, also known as autosomal dominant nonsyndromic deafness 16, is related to deafness, autosomal dominant 7 and deafness, autosomal dominant 4a. An important gene associated with Deafness, Autosomal Dominant 16 is STRC (Stereocilin), and among its related pathways/superpathways is Sensory processing of sound. Related phenotypes are tinnitus and adult onset sensorineural hearing impairment

Related ID：

MALACARDS：DFN148

OMIM：603964