FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Creutzfeldt-Jakob disease ID (Ontology) DOID:11949 (Human Disease)
Definition
Also Known As "CJD" ; "Creutzfeldt Jacob syndrome" ; "Creutzfeldt Jakob disease" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       7
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 Creutzfeldt-Jakob disease       7      5      1
 ameliorates | Creutzfeldt-Jakob disease       2       --       --
 exacerbates | Creutzfeldt-Jakob disease       2       --       --
 model of | Creutzfeldt-Jakob disease       3       --       --
Spanning Tree (Parents/Children)
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disease by infectious agent__
brain disease________________|
                             prion disease
                              |__Creutzfeldt-Jakob disease  13 rec.
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Synonyms
  • "CJD" EXACT OMO:0003012
    "Creutzfeldt Jacob syndrome" EXACT
    "Creutzfeldt Jakob disease" EXACT
    "Creutzfeldt-Jacob disease" EXACT
    "Jakob-Creutzfeldt disease" EXACT
    "Subacute spongiform encephalopathy" EXACT
    "Transmissible virus dementia" EXACT
Secondary IDs
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EFO:0004226
GARD:6956
ICD10CM:A81.0
ICD9CM:046.1
MESH:D007562
MIM:123400
NCI:C26802
SNOMEDCT_US_2023_03_01:155061007
UMLS_CUI:C0022336