Deafness, Autosomal Recessive 18b (DFNB18B)

Alias:

Dfnb18b

Autosomal Recessive Nonsyndromic Deafness 18b

Autosomal Recessive Nonsyndromic Hearing Loss 18b

Deafness, Autosomal Recessive, Type 18b

Deafness, Autosomal Recessive, 18b

Autosomal Recessive Deafness 18b

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 18b, also known as dfnb18b, is related to deafness, autosomal dominant 4b and peripheral vertigo. An important gene associated with Deafness, Autosomal Recessive 18b is OTOG (Otogelin), and among its related pathways/superpathways is Sensory processing of sound. Related phenotypes are sensorineural hearing impairment and vestibular hypofunction

Related ID：

MALACARDS：DFN248

OMIM：614945

MESH：D034381