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
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.