Deafness, Autosomal Recessive 61 (DFNB61)

Alias:

Dfnb61

Autosomal Recessive Nonsyndromic Deafness 61

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 61

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 61

Autosomal Recessive Nonsyndromic Hearing Loss 61

Deafness, Autosomal Recessive, Type 61

Deafness, Autosomal Recessive, 61

Autosomal Recessive Deafness 61

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 61, also known as dfnb61, is related to nonsyndromic hearing loss and deafness, autosomal dominant 3b. An important gene associated with Deafness, Autosomal Recessive 61 is SLC26A5 (Solute Carrier Family 26 Member 5), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and nervous system

Related ID：

MALACARDS：DFN188

OMIM：613865

MESH：D006319