ORPHA:264694
Interstitial lung disease specific to infancy
Synonyms: ILD specific to infancy
- 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 infancy | ILD specific to infancy |
| fr | Pneumopathie interstitielle spécifique de la petite enfance | ILD spécifique de la petite enfance |
| de | Interstitielle Lungenkrankheit, spezifische, des Kleinkindes | ILD des Kleinkindes |
| es | Enfermedad pulmonar intersticial específica del lactante | EPI específica del lactante |
| it | Pneumopatia interstiziale specifica dell'infanzia | ILD specifica dell'infanzia |
| nl | Interstitiële longziekte specifiek voor de kleuterjaren | ILD specifiek voor de kleuterjaren |
| pt | Doença pulmonar intersticial específica da infância | |
| pl | Śródmiąższowa choroba płuc specyficzna dla wieku niemowlęcego | ILD specyficzna dla wieku niemowlęcego |
| cs | Intersticiální plicní nemoc specifická pro kojence | ILD specifická pro kojence |
| uk | Інтерстиціальна хвороба легень, характерна для немовлят | ILD, специфічна для немовлят |
| zh | 婴儿期特有的间质性肺病 | 婴儿期特有的ILD |
| tr | Süt çocuğunda interstisyel akciğer hastalığı | Bebeklik dönemine özgü ILD |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017019 | E | validated | |
| MONDO | 17019 | E | validated | |
| UMLS | C5679737 | 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:264665Primary interstitial lung disease specific to childhood
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/264694
- This record as JSON: /data/d/264694.json