ORPHA:309028
Disorder of lipid absorption and transport
- 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 | Disorder of lipid absorption and transport | |
| fr | Trouble du transport et de l'absorption des lipides | |
| de | Fettstoffwechsel-Störung | |
| es | Trastornos de absorción y transporte de lípidos | |
| it | Difetto dell'assorbimento e del trasporto dei lipidi | |
| nl | Stoornis van lipidenabsorptie en transport | |
| pt | Alteração da absorção lipídica e transporte | |
| pl | Zaburzenia wchłaniania i transportu lipidów | |
| cs | Poruchy absorpce a transportu lipidů | |
| uk | Порушення всмоктування та транспортування ліпідів | |
| zh | 脂质吸收-转运障碍 | |
| tr | Lipid emilimi ve taşınması bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C62 | E | specific | validated |
| MONDO | 17709 | E | validated | |
| UMLS | C5681072 | 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 (3):
- ORPHA:309005Disorder of lipid metabolism
rare inborn errors of metabolism; rare genetic diseases - ORPHA:165661Genetic pancreatic disease
rare genetic diseases - ORPHA:101937Rare pancreatic disease
rare gastroenterological diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/309028
- This record as JSON: /data/d/309028.json