Deafness, Autosomal Recessive 79 (DFNB79)

Alias:

Dfnb79

Autosomal Recessive Nonsyndromic Deafness 79

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 79

Autosomal Recessive Nonsyndromic Hearing Loss 79

Deafness, Autosomal Recessive, Type 79

Deafness, Autosomal Recessive, 79

Autosomal Recessive Deafness 79

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 79, also known as dfnb79, is related to nonsyndromic hearing loss and sensorineural hearing loss. An important gene associated with Deafness, Autosomal Recessive 79 is TPRN (Taperin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Related phenotypes are delayed speech and language development and sensorineural hearing impairment

Related ID：

MALACARDS：DFN123

OMIM：613307

MESH：D006319