Acquired Creutzfeldt-Jakob disease
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A group of human prion diseases characterized by progressive, invariably fatal neurodegeneration resulting from accidental transmission of prions. The group comprises iatrogenic Creutzfeldt-Jakob disease (CJD), which results from transmission of CJD prions in the course of medical procedures or treatments, and variant CJD (transmission via consumption of products from prion-diseased cows or via blood transfusion from an affected individual).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired Creutzfeldt-Jakob disease | |
| fr | Maladie de Creutzfeldt-Jakob acquise | |
| de | Creutzfeldt-Jakob-Krankheit, erworbene | |
| es | Enfermedad de Creutzfeldt-Jakob adquirida | |
| it | Malattia di Creutzfeldt-Jakob acquisita | |
| nl | Verworven ziekte van Creutzfeldt-Jakob | |
| pt | Doença adquirida de Creutzfeldt-Jakob | |
| pl | Nabyta choroba Creutzfeldta i Jakoba | |
| cs | Získaná Creutzfeldtova-Jakobova choroba | Získaná Creutzfeldt-Jakobova choroba |
| uk | Набута хвороба Крейтцфельдта-Якоба | |
| zh | 获得性克雅氏病 | |
| tr | Edinsel Creutzfeldt-Jakob hastalığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 123400 | NTBT | validated | |
| MONDO | 0018686 | E | validated | |
| MONDO | 18686 | E | validated | |
| UMLS | C5681100 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:576360Acquired human prion disease
rare neurological diseases - ORPHA:306695Miscellaneous movement disorder due to neurodegenerative disease
rare neurological diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Europe | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/454700
- This record as JSON: /data/d/454700.json