Deafness, Autosomal Dominant 76 (DFNA76)

Alias:

Dfna76

Hearing Loss, Autosomal Dominant 76

Deafness, Autosomal Dominant, 76

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 76, also known as dfna76, is related to autosomal dominant nonsyndromic deafness 76. An important gene associated with Deafness, Autosomal Dominant 76 is PLS1 (Plastin 1). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN382

OMIM：618787

MESH：D034381