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Summary Literature (0)
OMIM:123400 - CREUTZFELDT-JAKOB DISEASE; CJD


Xenbase Genes: prnp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007403 - inherited Creutzfeldt-Jakob disease
MONDO:0016079 - sporadic Creutzfeldt-Jakob disease
MONDO:0018686 - acquired Creutzfeldt-Jakob disease

Disease Ontology (DO):
DOID:11949 - Creutzfeldt-Jakob disease