Deafness, Autosomal Dominant 52 (DFNA52)

Deafness, Autosomal Dominant 52(来自ICD-11)

别称:

Autosomal Dominant Nonsyndromic Deafness 52

Dfna52

Deafness, Autosomal Dominant 42

Autosomal Dominant Deafness 52

Dfna42

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 52, also known as autosomal dominant nonsyndromic deafness 52, is related to sensorineural hearing loss. An important gene associated with Deafness, Autosomal Dominant 52 is DFNA42 (Deafness, Autosomal Dominant 42). Related phenotypes are hearing impairment and Increased shRNA abundance (Z-score > 2)

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