Deafness, Autosomal Recessive 16 (DFNB16)

Alias:

Dfnb16

Autosomal Recessive Nonsyndromic Deafness 16

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 16

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 16

Autosomal Recessive Nonsyndromic Hearing Loss 16

Deafness, Autosomal Recessive, Type 16

Deafness, Autosomal Recessive, 16

Autosomal Recessive Deafness 16

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 16, also known as dfnb16, is related to deafness-infertility syndrome and vertigo, benign recurrent. An important gene associated with Deafness, Autosomal Recessive 16 is STRC (Stereocilin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and nervous system

Related ID：

MALACARDS：DFN143

OMIM：603720

MESH：D006319