Deafness, Autosomal Dominant 5 (DFNA5)

Alias:

Dfna5

Autosomal Dominant Nonsyndromic Deafness 5

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 5

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 5

Autosomal Dominant Nonsyndromic Hearing Loss 5

Deafness, Autosomal Dominant, Type 5

Deafness, Autosomal Dominant, 5

Autosomal Dominant Deafness 5

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 5, also known as dfna5, is related to autosomal dominant nonsyndromic deafness and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 5 is GSDME (Gasdermin E). Affiliated tissues include brain and breast.

Related ID：

MALACARDS：DFN159

OMIM：600994

MESH：D006319