ORPHA:275853
Syndrome with pulmonary hypertension as a major feature
- 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 | Syndrome with pulmonary hypertension as a major feature | |
| fr | Syndrome avec une hypertension pulmonaire comme manifestation majeure | |
| de | Syndrom mit pulmonaler Hypertonie als Hauptmerkmal | Syndrom mit pulmonaler Hypertension als Hauptmerkmal |
| es | Síndrome con hipertensión pulmonar como característica principal | |
| it | Sindrome con ipertensione polmonare come segno cardinale | |
| nl | Syndroom met pulmonale hypertensie als hoofdkenmerk | |
| pt | Síndrome com hipertensão pulmonar como característica principal | |
| pl | Zespół z nadciśnieniem płucnym jako głównym objawem | |
| cs | Syndrom s plicní hypertenzí jako hlavním příznakem | |
| uk | Синдром легеневої гіпертензії, як основний синдром | |
| zh | 以肺动脉高压为主要特征的综合征 | |
| tr | Esas klinik özelliği pulmoner hipertansiyon olan sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17159 | E | validated | |
| UMLS | C5680755 | 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:71198Rare pulmonary hypertension
rare respiratory diseases
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Genes
0 directOrphanet records no gene directly on this code.
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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/275853
- This record as JSON: /data/d/275853.json