Search Ontology:
Human Disease

familial hemiplegic migraine 3

Term ID
DOID:0111183
Synonyms
  • FHM3
  • MHP3
Definition
A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3. https://www.ncbi.nlm.nih.gov/pubmed/16054936
References
Ontology
Human Disease   ( DOID:0111183 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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