Deafness, Autosomal Dominant 28 (DFNA28)

Alias:

Dfna28

Autosomal Dominant Nonsyndromic Deafness 28

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 28

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 28

Autosomal Dominant Nonsyndromic Hearing Loss 28

Deafness, Autosomal Dominant, Type 28

Deafness, Autosomal Dominant, 28

Autosomal Dominant Deafness 28

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 28, also known as dfna28, is related to sensorineural hearing loss and autosomal dominant nonsyndromic deafness. An important gene associated with Deafness, Autosomal Dominant 28 is GRHL2 (Grainyhead Like Transcription Factor 2). Affiliated tissues include brain, and related phenotypes are Increased shRNA abundance (Z-score > 2) and hearing/vestibular/ear

Related ID：

MALACARDS：DFN094

OMIM：608641

MESH：D006319