Deafness, Autosomal Dominant 43 (DFNA43)

Alias:

Dfna43

Autosomal Dominant Nonsyndromic Deafness 43

Autosomal Dominant Deafness 43

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 43, also known as dfna43, is related to deafness, autosomal dominant 40 and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 43 is DFNA43 (Deafness, Autosomal Dominant 43). Related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN156

OMIM：608394