ORPHA:101953
Rare 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare dyslipidemia | |
| fr | Dyslipidémie rare | |
| de | Dyslipidämie, seltene | |
| es | Dislipidemia rara | |
| it | Dislipidemia rara | |
| nl | Zeldzame dyslipidemie | |
| pt | Dislipidemia rara | |
| pl | Rzadkie dyslipidemie | |
| cs | Vzácná dyslipidémie | |
| uk | Рідкісна дисліпідемія | |
| zh | 罕见血脂异常 | |
| tr | Nadir dislipidemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15123 | E | validated | |
| UMLS | C5681798 | E | validated | |
| GARD | 19797 | 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 (3):
- ORPHA:309005Disorder of lipid metabolism
rare inborn errors of metabolism; rare genetic diseases - ORPHA:97978Rare endocrine disease
rare endocrine diseases - ORPHA:156638Rare genetic endocrine disease
rare genetic 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101953
- This record as JSON: /data/d/101953.json