epilepsy, myoclonic, infantile, severe

Preferred Label : epilepsy, myoclonic, infantile, severe;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0334943;

UMLS CUI

C0751122;

Automatic exact mappings (from CISMeF team)
- Developmental and Epileptic Encephalopathy 2 [NCIt concept]
CISMeF manual mappings
- Dravet syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Developmental and Epileptic Encephalopathy 6A [NCIt concept]
- Dravet Syndrome [NCIt concept]
- Dravet syndrome [MedDRA LLT]
- Dravet syndrome [PASCAL descriptor]
- Dravet syndrome [DO Concept]
- Dravet syndrome [ICD-11 Sub-sub category]
- Dravet syndrome [DO Concept]
- Dravet syndrome [OMIM Phenotype]
- Severe myoclonic epilepsy in infancy (disorder) [SNOMED CT concept]
- Severe myoclonic epilepsy of infancy [MedDRA Preferred Term]
- severe myoclonic epilepsy of infancy [Disease (Nov.)]
Related record
- epilepsies, myoclonic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Developmental and Epileptic Encephalopathy 6A [NCIt concept]
- Dravet Syndrome [NCIt concept]
- Dravet syndrome [OMIM Phenotype]
- Dravet syndrome [MedDRA LLT]
- Dravet syndrome [ORDO Disease]
- Severe myoclonic epilepsy in infancy (disorder) [SNOMED CT concept]
- Severe myoclonic epilepsy of infancy [MedDRA Preferred Term]