Deafness, Autosomal Recessive 23 (DFNB23)

Alias:

Dfnb23

Autosomal Recessive Nonsyndromic Deafness 23

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 23

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 23

Autosomal Recessive Nonsyndromic Hearing Loss 23

Deafness, Autosomal Recessive, Type 23

Deafness, Autosomal Recessive, 23

Autosomal Recessive Deafness 23

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 23, also known as dfnb23, is related to usher syndrome, type if and deafness, autosomal recessive 1a. An important gene associated with Deafness, Autosomal Recessive 23 is PCDH15 (Protocadherin Related 15), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include brain and eye, and related phenotypes are sensorineural hearing impairment and visual impairment

Related ID：

MALACARDS：DFN093

OMIM：609533

MESH：D006319