Deafness, Autosomal Recessive 8 (DFNB8)

Alias:

Neurosensory Nonsyndromic Recessive Deafness 8

Dfnb10

Dfnb8

Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8

Autosomal Recessive Nonsyndromic Deafness 8

Deafness, Autosomal Recessive 10

Nsrd8

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 8

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 8

Childhood-Onset Neurosensory Autosomal Recessive Deafness 8

Childhood-Onset Neurosensory Deafness Autosomal Recessive 8

Autosomal Recessive Nonsyndromic Hearing Loss 8

Deafness Neurosensory Autosomal Recessive 8

Deafness, Autosomal Recessive, Type 8/10

Deafness, Autosomal Recessive 8/10

Deafness Autosomal Recessive 8/10

Deafness, Autosomal Recessive, 8

Autosomal Recessive Deafness 10

Deafness Autosomal Recessive 10

Autosomal Recessive Deafness 8

Nrsd8

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 8, also known as neurosensory nonsyndromic recessive deafness 8, is related to glycerol kinase deficiency and non-syndromic genetic deafness. An important gene associated with Deafness, Autosomal Recessive 8 is TMPRSS3 (Transmembrane Serine Protease 3), 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：DFN352

OMIM：601072

MESH：D006319