Temporal epilepsy, familial

Preferred Label : Temporal epilepsy, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531417;

UMLS CUI

C1842564;

Currated CISMeF NLP mapping
- Epilepsy, familial temporal lobe [OMIM phenotypic series]
- Familial temporal lobe epilepsy [ICD-11 More detail]
- Familial temporal lobe epilepsy [ORDO Disease]
- Familial temporal lobe epilepsy (disorder) [SNOMED CT concept]
Related record
- temporal epilepsy, familial [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Epilepsy, familial temporal lobe, 2 [OMIM Phenotype]
- Familial temporal lobe epilepsy [ORDO Disease]
- Familial temporal lobe epilepsy (disorder) [SNOMED CT concept]
- familial temporal lobe epilepsy 2 [DO Concept]
Validated automatic mappings to BTNT
- Epilepsy, familial temporal lobe, 2 [OMIM Phenotype]
- familial temporal lobe epilepsy 2 [DO Concept]