familial progressive myoclonic epilepsy

Preferred Label : familial progressive myoclonic epilepsy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0335760;

UMLS CUI

C0751777;

Automatic exact mappings (from CISMeF team)
- Myoclonic epilepsy, progressive [HPO term]
- progressive myoclonic epilepsy [SNOMED Notion]
Related record
- myoclonic epilepsies, progressive [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]