Deafness, Autosomal Dominant 65 (DFNA65)

Alias:

Dfna65

Autosomal Dominant Nonsyndromic Deafness 65

Autosomal Dominant Nonsyndromic Hearing Loss 65

Deafness, Autosomal Dominant, Type 65

Deafness, Autosomal Dominant, 65

Autosomal Dominant Deafness 65

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 65, also known as dfna65, is related to deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Dominant 65 is TBC1D24 (TBC1 Domain Family Member 24). Affiliated tissues include brain, and related phenotypes are progressive hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN278

OMIM：616044

MESH：D006319