Migraine, Familial Hemiplegic, 3 (FHM3)

Migraine, Familial Hemiplegic, 3(来自ICD-11)
别称:
Fhm3
Familial Hemiplegic Migraine 3
Mhp3
Migraine, Hemiplegic, Familial, Type 3
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Migraine, Familial Hemiplegic, 3, also known as fhm3, is related to hemiplegia and migraine with aura, and has symptoms including hemiparesis, hemiplegia and photophobia. An important gene associated with Migraine, Familial Hemiplegic, 3 is SCN1A (Sodium Voltage-Gated Channel Alpha Subunit 1), and among its related pathways/superpathways are Activation of cAMP-Dependent PKA and Neuropathic Pain-Signaling in Dorsal Horn Neurons. Related phenotypes are migraine with aura and phonophobia
查看原文 参与反馈
相关ID:

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
AD
Unknown
--
20
254
14

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