Deafness, Autosomal Dominant 9 (DFNA9)

Alias:

Dfna9

Autosomal Dominant Nonsyndromic Deafness 9

Autosomal Dominant Nonsyndromic Hearing Loss 9

Deafness, Autosomal Dominant, Type 9

Deafness, Autosomal Dominant, 9

Autosomal Dominant Deafness 9

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 9, also known as dfna9, is related to meniere disease and vestibular disease, and has symptoms including tinnitus and vertigo. An important gene associated with Deafness, Autosomal Dominant 9 is COCH (Cochlin), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include bone, and related phenotypes are vertigo and tinnitus

Related ID：

MALACARDS：DFN136

OMIM：601369

MESH：D006319