ORPHA:178320
Acute lung injury
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acute lung injury | |
| fr | Agression pulmonaire aiguë | |
| de | Lungenverletzung, akute | |
| es | Lesión pulmonar aguda | |
| it | Lesione polmonare acuta | |
| nl | Acuut letsel van long | Acuut longletsel |
| pt | Lesão pulmonar aguda | |
| pl | Ostry uraz płuc | |
| cs | Akutní plicní poranění | |
| uk | Гостре пошкодження легень | |
| zh | 急性肺损伤 | |
| tr | Akut akciğer hasarı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | S27.3 | NTBT | attributed | validated |
| ICD-11 | NB32.3 | NTBT | attributed | validated |
| MONDO | 0015796 | E | validated | |
| MeSH | D055371 | E | validated | |
| UMLS | C0242488 | E | validated | |
| MedDRA | 10069351 | 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 (1):
- ORPHA:101944Rare pulmonary disease
rare respiratory diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
4 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-5 / 10 000 | 25 / 100 000 | Europe | Value and class | Not yet validated | 15659944[PMID]_15166842[PMID] |
| Point prevalence | 1-5 / 10 000 | — | Europe | Class only | Validated | European Medicines Agency 2012[OTHER] |
| Annual incidence | 1-5 / 10 000 | 25 / 100 000 | Australia | Value and class | Not yet validated | 15659944[PMID]_15166842[PMID] |
| Annual incidence | 6-9 / 10 000 | 65 / 100 000 | United States | Value and class | Not yet validated | 15659944[PMID]_20073554[PMID]_9468178[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
21 annotations · validated 2020-03-18| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0011112 | Abnormality of serum cytokine level | |
| HP:0002094 | Dyspnea | |
| HP:0011227 | Elevated circulating C-reactive protein concentration | |
| HP:0012418 | Hypoxemia | |
| HP:0030783 | Increased circulating interleukin 6 concentration | |
| HP:0032094 | Increased circulating surfactant protein level | |
| HP:0002090 | Pneumonia | |
| HP:0002113 | Pulmonary infiltrates | |
| HP:0002098 | Respiratory distress | |
| HP:0002878 | Respiratory failure | |
| HP:0002789 | Tachypnea | |
| Occasional (29-5%) | ||
| HP:0006530 | Abnormal pulmonary interstitial morphology | |
| HP:0011118 | Abnormality of tumor necrosis factor secretion | |
| HP:0001735 | Acute pancreatitis | |
| HP:0030955 | Alcoholism | |
| HP:0025420 | Diffuse alveolar hemorrhage | |
| HP:0000969 | Edema | |
| HP:0001945 | Fever | |
| HP:0002105 | Hemoptysis | |
| HP:0100806 | Sepsis | |
| HP:0031273 | Shock | |
Annotation source: 27652982[PMID]_22268322[PMID]_25466727[PMID]
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/178320
- This record as JSON: /data/d/178320.json