Deafness, Autosomal Dominant 86 (DFNA86)

Alias:

Dfna86

Hearing Loss, Autosomal Dominant 86

Deafness, Autosomal Dominant, 86

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 86, is also known as dfna86. An important gene associated with Deafness, Autosomal Dominant 86 is THOC1 (THO Complex Subunit 1). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN402

OMIM：620280

MESH：D006319