ORPHA:156629
Rare genetic 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 genetic cause of hypertension | |
| fr | Hypertension artérielle de cause génétique rare | |
| de | Hypertension, genetisch bedingte | |
| es | Hipertensión genética | |
| it | Ipertensione genetica | |
| nl | Genetische hypertensie | |
| pt | Hipertensão genética | |
| pl | Nadciśnienie uwarunkowane genetycznie | |
| cs | Geneticky podmíněná hypertenze | |
| uk | Рідкісна генетично обумовлена гіпертонія | |
| zh | 罕见遗传性高血压 | |
| tr | Hipertansiyonun nadir genetik nedeni |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15512 | E | validated | |
| UMLS | C5680639 | 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 (2):
- ORPHA:93618Rare cause of hypertension
rare renal diseases - ORPHA:98056Rare genetic renal disease
rare genetic diseases
Children (10):
- ORPHA:320Apparent mineralocorticoid excess
- ORPHA:88659Autosomal dominant progressive nephropathy with hypertension
- ORPHA:1276Brachydactyly-arterial hypertension syndrome
- ORPHA:235936Familial hyperaldosteronism
- ORPHA:88660Hypertension due to gain-of-function mutations in the mineralocorticoid receptor
- ORPHA:526Liddle syndrome
- ORPHA:636Neurofibromatosis type 1
- ORPHA:757Pseudohypoaldosteronism type 2
- ORPHA:758Pseudoxanthoma elasticum
- ORPHA:904Williams syndrome
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/156629
- This record as JSON: /data/d/156629.json