Deafness, Autosomal Dominant 4b (DFNA4B)

Deafness, Autosomal Dominant 4b(来自ICD-11)

别称:

Dfna4b

Autosomal Dominant Nonsyndromic Deafness 4b

Autosomal Dominant Nonsyndromic Hearing Loss 4b

Deafness, Autosomal Dominant, Type 4b

Deafness, Autosomal Dominant, 4b

Autosomal Dominant Deafness 4b

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 4b, also known as dfna4b, is related to non-syndromic genetic deafness and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Dominant 4b is CEACAM16 (CEA Cell Adhesion Molecule 16, Tectorial Membrane Component), and among its related pathways/superpathways is Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and visual impairment

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