ORPHA:71198
Rare pulmonary 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare pulmonary hypertension | |
| fr | Hypertension pulmonaire rare | |
| de | Pulmonale Hypertonie, seltene | Hypertension, pulmonale |
| es | Hipertensión pulmonar rara | |
| it | Ipertensione polmonare | |
| nl | Zeldzame pulmonale hypertensie | |
| pt | Hipertensão pulmonar, rara | |
| pl | Rzadkie nadciśnienie płucne | |
| cs | Vzácná plicní hypertenze | |
| uk | Рідкісна легенева гіпертензія | |
| zh | 罕见肺性高血压 | |
| tr | Nadir pulmoner hipertansiyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19096 | E | validated | |
| UMLS | C5681268 | 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 (1):
- ORPHA:97955Rare respiratory disease
rare respiratory diseases
Children (6):
- ORPHA:70591Chronic thromboembolic pulmonary hypertension
- ORPHA:182090Pulmonary arterial hypertension
- ORPHA:275837Pulmonary hypertension owing to lung disease and/or hypoxia
- ORPHA:275844Pulmonary hypertension with unclear multifactorial mechanism
- ORPHA:431353Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis
- ORPHA:275853Syndrome with pulmonary hypertension as a major feature
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_25385937[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/71198
- This record as JSON: /data/d/71198.json