Deafness, Autosomal Dominant 11 (DFNA11)

Alias:

Dfna11

Autosomal Dominant Nonsyndromic Deafness 11

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 11

Autosomal Dominant Nonsyndromic Hearing Loss 11

Deafness, Autosomal Dominant, Type 11

Deafness, Autosomal Dominant, 11

Autosomal Dominant Deafness 11

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 11, also known as dfna11, is related to retinal degeneration and rare genetic deafness. An important gene associated with Deafness, Autosomal Dominant 11 is MYO7A (Myosin VIIA), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sweet Taste Signaling. Affiliated tissues include brain, and related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：DFN251

OMIM：601317

MESH：D006319