Deafness, Autosomal Dominant 82 (DFNA82)

Alias:

Dfna82

Hearing Loss, Autosomal Dominant 82

Deafness, Autosomal Dominant, 82

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 82, is also known as dfna82. An important gene associated with Deafness, Autosomal Dominant 82 is ATP2B2 (ATPase Plasma Membrane Ca2+ Transporting 2). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN395

OMIM：619804

MESH：D006319