spongiform encephalopathy with neuropsychiatric features

Preferred Label : spongiform encephalopathy with neuropsychiatric features;

MeSH note : mutations in PRNP;

Origin ID

C564678;

UMLS CUI

C1847650;

Currated CISMeF NLP mapping
- Spongiform encephalopathy with neuropsychiatric features [OMIM Phenotype]
MeSH term(s) associated for indexing
- heredodegenerative disorders, nervous system [MeSH Descriptor]
- mental disorders [MeSH Descriptor]
- prion diseases [MeSH Descriptor]
Record concept(s)
- spongiform encephalopathy with neuropsychiatric features [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spongiform encephalopathy with neuropsychiatric features [OMIM Phenotype]