ORPHA:181422
Rare hyperlipidemia
- 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 | Rare hyperlipidemia | |
| fr | Hyperlipidémie rare | |
| de | Hyperlipidämie, seltene | |
| es | Hiperlipidemia rara | Hiperlipemia rara · Hiperlipidosis rara |
| it | Iperlipidemia rara | |
| nl | Zeldzame hyperlipidemie | |
| pt | Hiperlipidemia rara | |
| pl | Rzadka hiperlipidemia | |
| cs | Vzácná hyperlipidémie | |
| uk | Рідкісна гіперліпідемія | |
| zh | 罕见高脂血症 | |
| tr | Nadir hiperlipidemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15901 | E | validated | |
| UMLS | C5680607 | 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:101953Rare dyslipidemia
rare inborn errors of metabolism; rare genetic diseases; rare endocrine diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:79211OBSOLETE: Combined hyperlipidemia referred to · inactive
- ORPHA:181425OBSOLETE: Rare major hypertriglyceridemia referred to · inactive
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/181422
- This record as JSON: /data/d/181422.json