Toxic oil syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Toxic oil syndrome is a rare intoxication, due to consumption of a rapeseed oil denatured with aniline 2%, characterized by generalized vascular lesions affecting all organs and vessels (including veins and arteries) and presenting with severe incapacitating myalgias, marked peripheral eosinophilia and pulmonary infiltrates.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Toxic oil syndrome | |
| fr | Syndrome de l'huile toxique | Syndrome de l'huile frelatée |
| de | Toxisches Öl-Syndrom | Toxic-Oil-Syndrom |
| es | Síndrome del aceite tóxico | |
| it | Sindrome dell'olio tossico | |
| nl | Toxische olie-syndroom | |
| pt | Síndrome do óleo tóxico | |
| pl | Zespół toksycznego oleju | |
| cs | Syndrom toxického oleje | |
| uk | Синдром токсичного масла | |
| zh | 油毒综合征 | |
| tr | Zehirli yağ sendromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | X46 | NTBT | attributed | validated |
| ICD-11 | NE61 | NTBT | attributed | validated |
| MONDO | 0016421 | E | validated | |
| UMLS | C0409998 | E | validated | |
| MedDRA | 10051222 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:556508Rare disorder due to poisoning
rare disorders due to toxic effects
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_12192735[PMID] |
| Cases/families | 20000 cases | Worldwide | Case(s) | Validated | 12192735[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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/227972
- This record as JSON: /data/d/227972.json