ORPHA:104005
Intestinal disease due to fat malabsorption
- 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 | Intestinal disease due to fat malabsorption | |
| fr | Maladie intestinale due à une malabsorption des graisses | |
| de | Intestinale Krankheit durch Fettmalabsorption | |
| es | Enfermedad intestinal por una mala absorción de grasas | |
| it | Malattia intestinale da anomalia dell'assorbimento dei grassi | |
| nl | Darmziekte door vetmalabsorptie | |
| pt | Doença intestinal por má absorção de gordura | |
| pl | Choroba jelit z powodu złego wchłaniania tłuszczy | |
| cs | Střevní choroby způsobené malabsorpcí tuků | |
| uk | Захворювання кишечника через мальабсорбцію жирів | |
| zh | 脂肪吸收障碍所致肠病 | |
| tr | Yağ emilim bozukluğuna bağlı bağırsak hastalığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15180 | E | validated | |
| UMLS | C5681745 | E | validated | |
| GARD | 19843 | 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:117569Rare intestinal disease
rare gastroenterological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
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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/104005
- This record as JSON: /data/d/104005.json