ORPHA:182101
Idiopathic eosinophilic pneumonia
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic eosinophilic pneumonia | |
| fr | Pneumonie à éosinophiles idiopathique | |
| de | Pneumonie, eosinophile idiopathische | |
| es | Neumonía eosinofílica idiopática | |
| it | Polmonite eosinofila idiopatica | |
| nl | Idiopathische eosinofiele pneumonie | |
| pt | Pneumonia esinofílica | |
| pl | Idiopatyczne eozynofilowe zapalenie płuc | |
| cs | Idiopatická eozinofilní pneumonie | |
| uk | Ідіопатична еозинофільна пневмонія | |
| zh | 特发性嗜酸性粒细胞性肺炎 | |
| tr | İdiyopatik eozinofilik pnömoni |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | J82 | E | specific | validated |
| MONDO | 0015927 | E | validated | |
| MONDO | 15927 | E | validated | |
| UMLS | C3872845 | 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:264935Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder
rare respiratory diseases; rare transplant-related disorders
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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.
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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/182101
- This record as JSON: /data/d/182101.json