ORPHA:181437
Rare syndromic dyslipidemia
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare syndromic dyslipidemia | |
| fr | Dyslipidémie syndromique rare | |
| de | Dyslipidämie, seltene syndromale | |
| es | Dislipidemia sindrómica rara | |
| it | Dislipidemia sindromica rara | |
| nl | Zeldzame syndromale dyslipidemie | |
| pt | Dislipidemia sindromática rara | |
| pl | Rzadka dyslipidemia syndromiczna | |
| cs | Vzácné syndromové dyslipidémie | |
| uk | Рідкісна синдромна дисліпідемія | |
| zh | 罕见综合征性血脂异常 | |
| tr | Nadir sendromik dislipidemi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15905 | E | validated | |
| UMLS | C5680608 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:101953Rare dyslipidemia
rare inborn errors of metabolism; rare genetic diseases; rare endocrine diseases
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/181437
- This record as JSON: /data/d/181437.json