FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term familial hemiplegic migraine 2 ID (Ontology) DOID:0111182 (Human Disease)
Definition A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.
Also Known As "Familial hemiplegic migraine-2" ; "FHM2" ; "MHP2"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes Human Disease Models
 familial hemiplegic migraine 2       2      1
 for disease ribbon | familial hemiplegic migraine 2       2       --
 model of | familial hemiplegic migraine 2       2       --
Spanning Tree (Parents/Children)
Only view relationship: 
  migraine with aura
   |__familial hemiplegic migraine
       |__familial hemiplegic migraine 2  3 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a familial hemiplegic migraine
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Familial hemiplegic migraine-2" EXACT
    "FHM2" EXACT OMO:0003012
    "MHP2" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
GARD:10095
MIM:602481