Deafness, Autosomal Dominant 72 (DFNA72)

Alias:

Dfna72

Hearing Loss, Autosomal Dominant 72

Deafness, Autosomal Dominant, 72

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 72, is also known as dfna72. An important gene associated with Deafness, Autosomal Dominant 72 is SLC44A4 (Solute Carrier Family 44 Member 4). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN328

OMIM：617606

MESH：D006319