ORPHA:576356
Sporadic human prion disease
Synonyms: Idiopathic human prion disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sporadic human prion disease | Idiopathic human prion disease |
| fr | Maladie à prion humaine sporadique | Maladie à prion humaine idiopathique |
| de | Prionkrankheit, humane, sporadiche Form | |
| es | Enfermedad por priones humanos esporádica | |
| it | Malattia umana sporadica da prioni | Malattia umana idiopatica da prioni |
| nl | Sporadische humane prionziekte | |
| pt | Doença de priões humana esporádica | |
| pl | Sporadyczna ludzka choroba prionowa | Idiopatyczna ludzka choroba prionowa |
| cs | Sporadické lidské prionové onemocnění | = en |
| uk | Спорадична пріонна хвороба людини | Ідіопатичне пріонне захворювання людини |
| zh | 散发性人朊病毒病 | 特发性人朊病毒病 |
| tr | Sporadik insan prion hastalığı | İdiyopatik insan prion hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680356 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:56970Human prion disease
rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/576356
- This record as JSON: /data/d/576356.json