MeSH Browser

MeSH Supplementary: Creutzfeldt-Jakob Disease, Sporadic
Unique ID: C565143
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565143
Registry Numbers: 0
Heading Mapped to: *Creutzfeldt-Jakob Syndrome
Frequency: 298
Note: The most common type of Creutzfeldt-Jakob Syndrome (85% of cases), where the patient has no known risk factors for the disease, such as inherited PRNP mutations or exposure to animals with BOVINE SPONGIFORM ENCEPHALOPATHY. OMIM: 123400
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Creutzfeldt-Jakob Disease, Sporadic MeSH Supplementary Concept Data 2025