migraine, familial hemiplegic, 3

Preferred Label : migraine, familial hemiplegic, 3;

MeSH note : mutation in SCN1A;

Origin ID

C566500;

UMLS CUI

C1864987;

Automatic exact mappings (from CISMeF team)
- familial hemiplegic migraine 3 [DO Concept]
Currated CISMeF NLP mapping
- Familial hemiplegic migraine 3 [ICD-11 More detail]
- Familial hemiplegic migraine type 3 (disorder) [SNOMED CT concept]
- Migraine, familial hemiplegic, 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- migraine disorders [MeSH Descriptor]
Record concept(s)
- migraine, familial hemiplegic, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Migraine, familial hemiplegic, 3 [OMIM Phenotype]