Deafness, Autosomal Recessive 37 (DFNB37)

Deafness, Autosomal Recessive 37(来自ICD-11)

别称:

Dfnb37

Autosomal Recessive Nonsyndromic Deafness 37

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 37

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 37

Congenital Neurosensory Deafness Autosomal Recessive 37

Autosomal Recessive Nonsyndromic Hearing Loss 37

Deafness, Autosomal Recessive, Type 37

Deafness, Autosomal Recessive, 37

Autosomal Recessive Deafness 37

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 37, also known as dfnb37, is related to rare genetic deafness and deafness, autosomal dominant 22. An important gene associated with Deafness, Autosomal Recessive 37 is MYO6 (Myosin VI), and among its related pathways/superpathways are ERK Signaling and Integrin Pathway. Affiliated tissues include eye and brain, and related phenotypes are sensorineural hearing impairment and rod-cone dystrophy

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