Deafness, Autosomal Dominant 77 (DFNA77)

Deafness, Autosomal Dominant 77(来自ICD-11)

别称:

Dfna77

Hearing Loss, Autosomal Dominant 77

Deafness, Autosomal Dominant, 77

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 77, also known as dfna77, is related to autosomal dominant nonsyndromic deafness 77. An important gene associated with Deafness, Autosomal Dominant 77 is ABCC1 (ATP Binding Cassette Subfamily C Member 1 (ABCC1 Blood Group)). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

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