A search in GWAS Central that returns a phenotype report annotated to MeSH disease Descriptor “Creutzfeldt-Jakob Syndrome” will display the mapping to the OMIM “Creutzfeldt-Jakob Disease” entry and the HPO-to-OMIM derived phenotypic abnormalities for the disease, which include “Confusion” and “Loss of facial expression”, amongst others (Figure 3). This evidence concerns the gene GFER and Creutzfeldt Jacob disease.