ORPHA:264735
Interstitial lung disease specific to adulthood
Synonyms: ILD specific to adulthood
- 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 | Interstitial lung disease specific to adulthood | ILD specific to adulthood |
| fr | Pneumopathie interstitielle spécifique de l'adulte | ILD spécifique de l'adulte |
| de | Interstitielle Lungenkrankheit des Erwachsenen | ILD des Erwachsenen |
| es | Enfermedad pulmonar intersticial específica del adulto | EPI específica del adulto |
| it | Pneumopatia interstiziale specifica dell'età adulta | ILD specifica dell'età adulta |
| nl | Interstitiële longziekte specifiek voor de volwassenheid | ILD specifiek voor de volwassenheid |
| pt | Doença pulmonar intersticial específica do adulto | |
| pl | Śródmiąższowa choroba płuc specyficzna dla wieku dorosłego | ILD specyficzne dla wieku dorosłego |
| cs | Intersticiální plicní nemoc specifická pro dospělé | ILD specifická pro dospělé |
| uk | Інтерстиціальне захворювання легень, характерне для дорослого віку | ILD, специфічна для дорослого віку |
| zh | 成年期特有的间质性肺病 | 成年期特有的ILD |
| tr | Yetişkinlik çağı interstisyel akciğer hastalığı | Erişkinliğe özgü ILD |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017026 | E | validated | |
| MONDO | 17026 | E | validated | |
| UMLS | C5679743 | 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:182095Interstitial lung disease
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/264735
- This record as JSON: /data/d/264735.json