ORPHA:182098
Pneumoconiosis
- Type
- Clinical group
- 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 | Pneumoconiosis | |
| fr | Pneumoconiose | |
| de | Pneumokoniose | |
| es | Neumoconiosis | |
| it | Pneumoconiosi | |
| nl | Pneumoconiose | Stoflong |
| pt | Pneumoconiose | |
| pl | Pylica płuc | |
| cs | Pneumokoniózy | |
| uk | Пневмоконіоз | |
| zh | 尘肺 | |
| tr | Pnömokonyoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | CA60 | E | specific | validated |
| MONDO | 0015926 | E | validated | |
| MONDO | 15926 | E | validated | |
| MeSH | D011009 | E | validated | |
| UMLS | C0032273 | E | validated | |
| MedDRA | 10035653 | 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:264740Primary interstitial lung disease specific to adulthood
rare respiratory diseases; rare transplant-related disorders
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/182098
- This record as JSON: /data/d/182098.json