Deafness, Autosomal Dominant 17 (DFNA17)

Alias:

Dfna17

Autosomal Dominant Nonsyndromic Deafness 17

Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts

Autosomal Dominant Nonsyndromic Hearing Loss 17

Deafness, Autosomal Dominant, Type 17

Deafness, Autosomal Dominant, 17

Autosomal Dominant Deafness 17

Cochleosaccular Degeneration

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 17, also known as dfna17, is related to myh-9 related disease and labyrinthitis. An important gene associated with Deafness, Autosomal Dominant 17 is MYH9 (Myosin Heavy Chain 9), and among its related pathways/superpathways are ERK Signaling and Integrin Pathway. Affiliated tissues include bone and kidney, and related phenotypes are hearing impairment and abnormality of the nervous system

Related ID：

MALACARDS：DFN200

OMIM：603622

MESH：D006319