epilepsy, myoclonic, benign adult familial, type 2

Preferred Label : epilepsy, myoclonic, benign adult familial, type 2;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0564613;

UMLS CUI

C1842852;

Currated CISMeF NLP mapping
- Epilepsy, familial adult myoclonic, 2 [OMIM Phenotype]
Related record
- epilepsy, myoclonic, benign adult familial, type 2 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign adult familial myoclonic epilepsy [ORDO Disease]
- Epilepsy, familial adult myoclonic, 2 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Benign adult familial myoclonic epilepsy [ORDO Disease]