Deafness, Autosomal Recessive 91 (DFNB91)

Deafness, Autosomal Recessive 91(来自ICD-11)

别称:

Dfnb91

Autosomal Recessive Nonsyndromic Deafness 91

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 91

Autosomal Recessive Nonsyndromic Hearing Loss 91

Deafness, Autosomal Recessive, Type 91

Deafness, Autosomal Recessive, 91

Autosomal Recessive Deafness 91

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 91, also known as dfnb91, is related to sensorineural hearing loss and deafness, autosomal dominant 17. An important gene associated with Deafness, Autosomal Recessive 91 is SERPINB6 (Serpin Family B Member 6), and among its related pathways/superpathways are G-protein signaling G-Protein alpha-i signaling cascades and Myometrial relaxation and contraction pathways. Related phenotypes are progressive hearing impairment and nervous system

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