epilepsy, partial, with variable foci

Preferred Label : epilepsy, partial, with variable foci;

Origin ID

C565785;

UMLS CUI

C1858477;

Currated CISMeF NLP mapping
- Epilepsy, familial focal, with variable foci 1 [OMIM Phenotype]
- Familial focal epilepsy with variable foci [ICD-11 More detail]
- Familial focal epilepsy with variable foci [ORDO Disease]
- Familial focal epilepsy with variable foci (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- epilepsies, partial [MeSH Descriptor]
Record concept(s)
- epilepsy, partial, with variable foci [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Epilepsy, familial focal, with variable foci 1 [OMIM Phenotype]
- Familial focal epilepsy with variable foci [ORDO Disease]
- Familial focal epilepsy with variable foci (disorder) [SNOMED CT concept]