Deafness, Autosomal Recessive 2 (DFNB2)

Alias:

Dfnb2

Neurosensory Nonsyndromic Recessive Deafness 2

Autosomal Recessive Nonsyndromic Deafness 2

Nsrd2

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 2

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 2

Autosomal Recessive Nonsyndromic Hearing Loss 2

Deafness, Autosomal Recessive 2, Neurosensory

Deafness Neurosensory Autosomal Recessive 2

Deafness, Autosomal Recessive, Type 2

Deafness, Autosomal Recessive, 2

Autosomal Recessive Deafness 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 2, also known as dfnb2, is related to usher syndrome, type if and deafness, autosomal recessive 23, and has symptoms including vertigo An important gene associated with Deafness, Autosomal Recessive 2 is MYO7A (Myosin VIIA), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sweet Taste Signaling. Affiliated tissues include brain and retina, and related phenotypes are sensorineural hearing impairment and vertigo

Related ID：

MALACARDS：DFN250

OMIM：600060

MESH：D006319