Deafness, Autosomal Recessive 59 (DFNB59)

Alias:

Dfnb59

Autosomal Recessive Nonsyndromic Deafness 59

Autosomal Recessive Nonsyndromic Hearing Loss 59

Deafness, Autosomal Recessive, Type 59

Deafness, Autosomal Recessive, 59

Autosomal Recessive Deafness 59

Dfnb59 Auditory Neuropathy

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 59, also known as dfnb59, is related to rare genetic deafness and sensorineural hearing loss. An important gene associated with Deafness, Autosomal Recessive 59 is PJVK (Pejvakin), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include prostate and lung, and related phenotypes are sensorineural hearing impairment and Increased gamma-H2AX phosphorylation

Related ID：

MALACARDS：DFN178

OMIM：610220

MESH：D006319