Familial Hemiplegic Migraine

Alias:
Hemiplegic Migraine, Familial
Hemiplegic-Ophthalmoplegic Migraine
Hemiplegic Migraine Familial
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Hemiplegic Migraine, also known as hemiplegic migraine, familial, is related to migraine, familial hemiplegic, 1 and familial or sporadic hemiplegic migraine. An important gene associated with Familial Hemiplegic Migraine is ATP1A2 (ATPase Na+/K+ Transporting Subunit Alpha 2), and among its related pathways/superpathways are G-Beta Gamma Signaling and Myometrial relaxation and contraction pathways. The drugs Salmon calcitonin and Nitroglycerin have been mentioned in the context of this disorder. Affiliated tissues include eye and brain, and related phenotypes are Decreased viability after sindbis virus (SIN) dsTE12Q infection and nervous system
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
32
410
85

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top