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MIM:123400 - CREUTZFELDT-JAKOB DISEASE; CJD
Xenbase Genes: prnp
Human Disease Resource: OMIM
MONDO:0007403 - inherited Creutzfeldt-Jakob disease |
MONDO:0016079 - sporadic Creutzfeldt-Jakob disease |
MONDO:0018686 - acquired Creutzfeldt-Jakob disease |
DOID:11949 - Creutzfeldt-Jakob disease |