Deafness, Autosomal Dominant 66 (DFNA66)

Alias:

Dfna66

Autosomal Dominant Nonsyndromic Deafness 66

Autosomal Dominant Nonsyndromic Hearing Loss 66

Deafness, Autosomal Dominant, 66

Autosomal Dominant Deafness 66

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 66, is also known as dfna66. An important gene associated with Deafness, Autosomal Dominant 66 is CD164 (CD164 Molecule), and among its related pathways/superpathways is Gap junction trafficking. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN329

OMIM：616969

MESH：D006319