epilepsy, myoclonic, benign adult familial, type 1

Preferred Label : epilepsy, myoclonic, benign adult familial, type 1;

MeSH synonym : benign adult familial myoclonic epilepsy 1; FAME1; cortical tremor, familial; epilepsy, familial adult myoclonic, 1; BAFME1; cortical myoclonic tremor with epilepsy, familial;

Details

Origin ID

C563399;

UMLS CUI

C1832841;

Automatic exact mappings (from CISMeF team)
- familial adult myoclonic epilepsy [DO Concept]
- familial adult myoclonic epilepsy 1 [DO Concept]
Currated CISMeF NLP mapping
- Epilepsy, familial adult myoclonic, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- epilepsies, myoclonic [MeSH Descriptor]
Record concept(s)
- epilepsy, myoclonic, benign adult familial, type 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Epilepsy, familial adult myoclonic, 1 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Benign adult familial myoclonic epilepsy [ORDO Disease]
- Benign adult familial myoclonic epilepsy (disorder) [SNOMED CT concept]

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