Deafness, Autosomal Recessive 3 (DFNB3)

Alias:

Dfnb3

Neurosensory Nonsyndromic Recessive Deafness 3

Nsrd3

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 3

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 3

Autosomal Recessive Nonsyndromic Hearing Loss 3

Deafness Neurosensory Autosomal Recessive 3

Deafness, Autosomal Recessive, Type 3

Deafness, Autosomal Recessive, 3

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 3, also known as dfnb3, is related to autosomal recessive nonsyndromic deafness 3 and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Recessive 3 is MYO15A (Myosin XVA), and among its related pathways/superpathways are RhoGDI Pathway and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are profound sensorineural hearing impairment and hearing/vestibular/ear

Related ID：

MALACARDS：DFN201

OMIM：600316

MESH：D006319