ORPHA:93618
Rare cause of hypertension
- 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 | Rare cause of hypertension | |
| fr | Hypertension artérielle de cause rare | |
| de | Seltene Ursache der Hypertension | |
| es | Hipertensión por una causa rara | |
| it | Causa rara di ipertensione | |
| nl | Zeldzame oorzaak van hypertensie | |
| pt | Hipertensão | |
| pl | Rzadkie przyczyny nadciśnienia | |
| cs | Vzácné příčiny hypertenze | |
| uk | Рідкісна причина гіпертонії | |
| zh | 罕见原因高血压 | |
| tr | Hipertansiyonun nadir nedeni |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681618 | 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:93626Rare renal disease
rare renal diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:97599OBSOLETE: Arterial hypertension due to renal artery stenosis secondary to vasculitis referred to · inactive
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/93618
- This record as JSON: /data/d/93618.json