Sensorineural Hearing Loss

Sensorineural Hearing Loss(来自ICD-11)
别称:
Sensory Hearing Loss
Hearing Loss, Sensorineural
Perceptive Hearing Loss or Deafness
Sensorineural Hearing Loss Disorder
Hearing Loss, High-Frequency
High Frequency Hearing Loss
High-Frequency Hearing Loss
Hearing Loss High-Frequency
Hearing Loss Sensorineural
High Frequency Deafness
Perceptive Hearing Loss
Sensorineural Deafness
Deafness Sensorineural
Hearing Loss, Central
Central Hearing Loss
Perceptive Deafness
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Sensorineural Hearing Loss, also known as sensory hearing loss, is related to deafness, autosomal dominant 1, with or without thrombocytopenia and rare autosomal recessive non-syndromic sensorineural deafness type dfnb, and has symptoms including tinnitus An important gene associated with Sensorineural Hearing Loss is GJB2 (Gap Junction Protein Beta 2), and among its related pathways/superpathways are Sensory processing of sound and Aminoglycoside Ototoxicity Pathway, Adverse Drug Reaction. The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include bone and bone marrow, and related phenotypes are nervous system and hearing/vestibular/ear
查看原文 参与反馈
相关ID:
MESH:D006319

基础信息

遗传方式
发病时间
患病率/发病率
相关基因
相关模型
参考文献
MALACARDS
--
Unknown
--
276
2517
4

疾病表征

#
分类
表征
HPO概率
Orphanet概率
HPO来源
暂无相关数据

基因 & 突变

#
基因
作用分类
分值
突变数量
暂无相关数据

靶点药物

药物名称
CAS号
研发状态
临床阶段
暂无相关数据

疾病模型

类型
名称
MGI
相关基因
品系来源
文献数量
暂无相关数据

文献报道

标题
PMID
期刊
年代
IF
暂无数据
Wechat
Comparison
Al agent
Tutorials
Back to top