Search Ontology:
Human Disease

familial hemiplegic migraine 1

Term ID
DOID:0111181
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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