Ocular Motility Disease

Ocular Motility Disease(来自ICD-11)
别称:
Abnormality of Eye Movement
Ocular Motility Disorders
Disorder of Eye Movements
Eye Movement Disorders
Eye Movement Disorder
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ocular Motility Disease, also known as abnormality of eye movement, is related to congenital fibrosis of the extraocular muscles and esotropia, and has symptoms including eye manifestations, ophthalmoplegia and spasm of conjugate gaze. An important gene associated with Ocular Motility Disease is CBS (Cystathionine Beta-Synthase). The drugs Dopamine and Metamfetamine have been mentioned in the context of this disorder. Affiliated tissues include eye and brain, and related phenotypes are nervous system and cellular
查看原文 参与反馈
相关ID:
MESH:D015835

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
--
45
405
3

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