OBO ID: DOID:0111183
Term Name: familial hemiplegic migraine 3 Search Ontology:
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 familial hemiplegic migraine 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SCN1A Migraine, familial hemiplegic, 3 609634
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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