Search Ontology:
Human Disease

familial hemiplegic migraine 2

Term ID
DOID:0111182
Synonyms
  • Familial hemiplegic migraine-2
  • FHM2
  • MHP2
Definition
A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2. https://www.ncbi.nlm.nih.gov/pubmed/12539047
References
Ontology
Human Disease   ( DOID:0111182 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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