Familial Hemiplegic Migraine

Preferred Label : Familial Hemiplegic Migraine;

NCIt definition : A migraine disorder characterized by individual and family history of aura that includes motor weakness.;

Details

Origin ID

C117009;

UMLS CUI

C0338484;

Automatic exact mappings (from CISMeF team)
- Migraine, familial hemiplegic [OMIM phenotypic series]
- migraine with aura [MeSH Descriptor]
Currated CISMeF NLP mapping
- Familial hemiplegic migraine [PASCAL descriptor]
- Familial hemiplegic migraine [MedDRA Preferred Term]
- Familial hemiplegic migraine [ICD-11 More detail]
- Familial hemiplegic migraine (disorder) [SNOMED CT concept]
- familial hemiplegic migraine [DO Concept]
- familial hemiplegic migraine [MeSH concept]
- familial hemiplegic migraine [SNOMED Notion]
Has associated anatomic sites
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hemiplegic migraine [PASCAL descriptor]
- Familial hemiplegic migraine [MedDRA Preferred Term]
- Familial hemiplegic migraine (disorder) [SNOMED CT concept]
- familial hemiplegic migraine [SNOMED Notion]
- familial hemiplegic migraine [MeSH concept]
- familial hemiplegic migraine [Disease (Nov.)]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]

Keyword's position in hierarchy(ies) :

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