ORPHA:411
Hyperlipoproteinemia type 1
inactive · moved to ORPHA:444490Familial chylomicronemia syndrome
Synonyms: HLP type 1
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Familial chylomicronemia syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hyperlipoproteinemia type 1 | HLP type 1 |
| fr | Hyperlipoprotéinémie type 1 | = en |
| de | Hyperlipoproteinämie Typ 1 | HLP Typ 1 · Hyperchylomikronämie, familiäre · Lipoproteinlipase-Mangel |
| es | Hiperlipoproteinemia tipo 1 | HLP tipo 1 |
| it | Iperlipoproteinemia, tipo 1 | Iperchilomicronemia familiare |
| nl | Hyperlipoproteïnemie type 1 | = en |
| pt | Hiperlipoproteinemia tipo 1 | HLP tipo 1 |
| pl | Hiperlipoproteinemia typu 1 | Rodzinna hiperchylomikronemia |
| cs | Hyperlipoproteinémie, typ 1 | = en |
| uk | Гіперліпопротеїнемія, тип 1 | HLP тип 1 |
| zh | 1型高脂蛋白血症 | 高脂蛋白血症1型 |
| tr | Hiperlipoproteinemi tip 1 | HLP tip 1 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0023817 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/411
- This record as JSON: /data/d/411.json