OBO ID: DOID:0111181
Term Name: familial hemiplegic migraine 1 Search Ontology:
Synonyms:
  • familial hemiplegic migraine1 with progressive cerebellar ataxia
  • FHM1
  • MHP1
Definition: A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13. (2)
References:
Ontology: Human Disease   ( DOID:0111181 )
Relationships
is a type of:
OTHER familial hemiplegic migraine 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA1A Migraine, familial hemiplegic, 1 141500
Migraine, familial hemiplegic, 1, with progressive cerebellar ataxia 141500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.