Deafness, Autosomal Dominant 25 (DFNA25)

Alias:

Dfna25

Autosomal Dominant Nonsyndromic Deafness 25

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 25

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 25

Autosomal Dominant Nonsyndromic Hearing Loss 25

Deafness, Autosomal Dominant, Type 25

Deafness, Autosomal Dominant, 25

Autosomal Dominant Deafness 25

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 25, also known as dfna25, is related to nonsyndromic hearing loss and sensorineural hearing loss. An important gene associated with Deafness, Autosomal Dominant 25 is SLC17A8 (Solute Carrier Family 17 Member 8), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN189

OMIM：605583

MESH：D006319