Creutzfeldt-Jakob disease, heidenhain variant

Preferred Label : Creutzfeldt-Jakob disease, heidenhain variant;

Origin ID

C566981;

UMLS CUI

C1969957;

Automatic exact mappings (from CISMeF team)
- Creutzfeldt-jakob disease [OMIM Phenotype]
MeSH term(s) associated for indexing
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- vision disorders [MeSH Descriptor]
Record concept(s)
- Creutzfeldt-Jakob disease, heidenhain variant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]