ORPHA:363306
Genetic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic intestinal disease due to fat malabsorption | |
| fr | Maladie intestinale due à une malabsorption des graisses d'origine génétique | |
| de | Genetisch bedingte intestinale Krankheit durch Fettmalabsorption | |
| es | Enfermedad intestinal de origen genético por malabsorción de grasa | |
| it | Malattia intestinale genetica da malassorbimento dei grassi | |
| nl | Genetische intestinale ziekte door malabsorptie van vet | |
| pt | Doença intestinal genética devido à má absorção de gordura | |
| pl | Genetyczna choroba jelit spowodowana złym wchłanianiem tłuszczy | |
| cs | Geneticky podmíněné nemoci střev způsobené malabsorbcí tuků | |
| uk | Генетично обумовлене захворювання кишечника, зумовлене мальабсорбцією жирів | |
| zh | 脂肪吸收障碍所致遗传性肠道疾病 | |
| tr | Yağ emilim bozukluğuna bağlı genetik bağırsak hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680981 | 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:165655Genetic intestinal 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/363306
- This record as JSON: /data/d/363306.json