ORPHA:264656
Interstitial lung disease specific to childhood
Synonyms: ILD specific to childhood
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Interstitial lung disease specific to childhood | ILD specific to childhood |
| fr | Pneumopathie interstitielle spécifique de l'enfance | ILD spécifique de l'enfance |
| de | Interstitielle Lungenkrankheit, spezifische, der Kindheit | ILD der Kindheit |
| es | Enfermedad pulmonar intersticial específica de la infancia | EPI específica de la infancia |
| it | Pneumopatia interstiziale specifica del bambino | ILD specifica dell'infanzia |
| nl | Interstitiële longziekte specifiek voor de kinderjaren | ILD specifiek voor de kinderjaren |
| pt | Doença pulmonar intersticial específica para a infância | |
| pl | Śródmiąższowa choroba płuc specyficzna dla wieku dziecięcego | ILD specyficzna dla wieku dziecięcego |
| cs | Intersticiální plicní nemoc specifická pro dětství | ILD specifická pro dětství |
| uk | Інтерстиціальне захворювання легень, характерне для дитячого віку | ILD, специфічна для дитячого віку |
| zh | 儿童期特有的间质性肺病 | 儿童期特有的ILD |
| tr | Çocukluk çağı interstisyel akciğer hastalığı | Çocukluğa özgü ILD |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017014 | E | validated | |
| MONDO | 17014 | E | validated | |
| UMLS | C5679752 | 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
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/264656
- This record as JSON: /data/d/264656.json