ORPHA:182095
Interstitial lung disease
Synonyms: ILD
- 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 | ILD |
| fr | Pneumopathie interstitielle | = en |
| de | Interstitielle Lungenkrankheit | = en |
| es | Enfermedad pulmonar intersticial | EPI · ILD |
| it | Pneumopatia interstiziale | = en |
| nl | Interstitiële longziekte | = en |
| pt | Pulmonar intersticial, doença | |
| pl | Śródmiąższowa choroba płuc | = en |
| cs | Intersticiální plicní nemoci | = en |
| uk | Інтерстиціальне захворювання легень | = en |
| zh | 间质性肺病 | = en |
| tr | İnterstisyel akciğer hastalığı | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015925 | E | validated | |
| MONDO | 15925 | E | validated | |
| MeSH | D017563 | E | validated | |
| UMLS | C0206062 | E | validated | |
| MedDRA | 10022611 | 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 (2):
- ORPHA:506222Rare disorder potentially indicated for lung transplant
rare transplant-related disorders - ORPHA:101944Rare pulmonary disease
rare respiratory diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
5 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 4.1 / 100 000 | Denmark | Value and class | Validated | 24636811[PMID] |
| Annual incidence | 1-9 / 100 000 | 5.4 / 100 000 | Europe | Value and class | Not yet validated | 24636811[PMID] |
| Annual incidence | 1-9 / 100 000 | 7.6 / 100 000 | Spain | Value and class | Validated | 15127977[PMID] |
| Annual incidence | 1-9 / 100 000 | 4.63 / 100 000 | Greece | Value and class | Validated | 19345567[PMID] |
| Point prevalence | 1-5 / 10 000 | 17.3 / 100 000 | Greece | Value and class | Validated | 19345567[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/182095
- This record as JSON: /data/d/182095.json