epilepsy, progressive myoclonic 2B

Preferred Label : epilepsy, progressive myoclonic 2B;

Origin ID

C564976;

UMLS CUI

C1850764;

Automatic exact mappings (from CISMeF team)
- Myoclonic epilepsy of lafora 1 [OMIM Phenotype]
Currated CISMeF NLP mapping
- epilepsy, progressive myoclonic 2B [MeSH concept]
MeSH term(s) associated for indexing
- myoclonic epilepsies, progressive [MeSH Descriptor]
Record concept(s)
- epilepsy, progressive myoclonic 2B [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myoclonic epilepsy of lafora 2 [OMIM Phenotype]