ORPHA:576742
Genetic hemolytic uremic syndrome
Synonyms: Genetic HUS
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic hemolytic uremic syndrome | Genetic HUS |
| fr | Syndrome hémolytique et urémique d'origine génétique | SHU d'origine génétique |
| de | Hämolytisch-urämisches Syndrom, genetisch bedingtes | HUS, genetisch bedingt |
| es | Síndrome hemolítico urémico genético | SHU genético |
| it | Sindrome genetica emolitico-uremica | HUS genetica |
| nl | Genetisch hemolytisch-uremisch syndroom | Genetisch HUS |
| pt | Síndrome hemolítico urémico genético | |
| pl | Genetyczny hemolityczny zespół mocznicowy | = en |
| cs | Genetický hemolyticko-uremický syndrom | = en |
| uk | Генетично обумовлений гемолітико-уремічний синдром | Генетичний HUS |
| zh | 遗传性溶血性尿毒综合征 | = en |
| tr | Genetik hemolitik üremik sendrom | Genetik HUS |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680355 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:183589Genetic thrombotic microangiopathy
rare genetic diseases - ORPHA:182043Rare constitutional hemolytic anemia
rare genetic diseases; rare hematological diseases
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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/576742
- This record as JSON: /data/d/576742.json