Familial Hemiplegic Migraine-1

Preferred Label : Familial Hemiplegic Migraine-1;

NCIt synonyms : FHM1;

NCIt definition : An autosomal dominant subtype of familial hemiplegic migraine caused by mutation(s) in the CACNA1A gene, encoding voltage-dependent P/Q-type calcium channel subunit alpha-1A.;

Details

Origin ID

C189277;

UMLS CUI

C1832884;

Currated CISMeF NLP mapping
- Familial hemiplegic migraine type 1 (disorder) [SNOMED CT concept]
- Migraine, familial hemiplegic, 1 [OMIM Phenotype]
- familial hemiplegic migraine 1 [DO Concept]
- familial hemiplegic migraine type 1 [Disease (Nov.)]
- hemiplegic migraine, familial type 1 [MeSH Supplementary Concept]
- hemiplegic migraine, familial type 1 [MeSH concept]
Has associated anatomic sites
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hemiplegic migraine type 1 (disorder) [SNOMED CT concept]
- Migraine, familial hemiplegic, 1 [OMIM Phenotype]
- familial hemiplegic migraine type 1 [Disease (Nov.)]
- hemiplegic migraine, familial type 1 [MeSH Supplementary Concept]
- hemiplegic migraine, familial type 1 [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- CACNA1A Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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