Deafness, Autosomal Dominant 71 (DFNA71)

Alias:

Dfna71

Hearing Loss, Autosomal Dominant 71

Deafness, Autosomal Dominant, 71

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 71, also known as dfna71, is related to contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 71 is DMXL2 (Dmx Like 2). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN335

OMIM：617605

MESH：D006319