ORPHA:97962
Rare surgical thoracic disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 surgical thoracic disease | |
| fr | Maladie rare en chirurgie thoracique | |
| de | Seltene Krankheit der Thoraxchirurgie | |
| es | Enfermedad torácica quirúrgica rara | |
| it | Malattia toracica rara d'interesse chirurgico | |
| nl | Zeldzame chirurgische thoracale ziekte | |
| pt | Doença torácica cirúrgica rara | |
| pl | Rzadkie operacyjne choroby klatki piersiowej | |
| cs | Vzácná chirurgická onemocnění hrudníku | |
| uk | Рідкісне хірургічне захворювання грудної клітки | |
| zh | 罕见胸外科疾病 | |
| tr | Nadir cerrahi torasik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681557 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Children (6):
- ORPHA:180776Non-syndromic diaphragmatic or thoracic malformation
- ORPHA:108993Non-syndromic respiratory or mediastinal malformation
- ORPHA:285014Rare disease with thoracic aortic aneurysm and aortic dissection
- ORPHA:180779Syndromic diaphragmatic or thoracic malformation
- ORPHA:108995Syndromic respiratory or mediastinal malformation
- ORPHA:97330Thoracic outlet 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/97962
- This record as JSON: /data/d/97962.json