Deafness, Autosomal Dominant 40 (DFNA40)

Alias:

Dfna40

Autosomal Dominant Nonsyndromic Deafness 40

Autosomal Dominant Nonsyndromic Hearing Loss 40

Deafness, Autosomal Dominant, Type 40

Deafness, Autosomal Dominant, 40

Autosomal Dominant Deafness 40

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 40, also known as dfna40, is related to autosomal dominant nonsyndromic deafness. An important gene associated with Deafness, Autosomal Dominant 40 is CRYM (Crystallin Mu). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN134

OMIM：616357

MESH：D006319