spastic paraplegia with myoclonic epilepsy

Preferred Label : spastic paraplegia with myoclonic epilepsy;

Origin ID

C564810;

UMLS CUI

C1849114;

Currated CISMeF NLP mapping
- Spastic paraplegia with myoclonic epilepsy [OMIM Phenotype]
MeSH term(s) associated for indexing
- epilepsies, myoclonic [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia with myoclonic epilepsy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic paraplegia with myoclonic epilepsy [OMIM Phenotype]