ORPHA:309824
Disorder of metabolite 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disorder of metabolite absorption and transport | |
| fr | Anomalie de transport et d'absorption des métabolites | |
| de | Metabolitenstoffwechsel- und Transportstörungen | |
| es | Trastornos de absorción y transporte de metabolitos | |
| it | Difetto del trasporto e dell'assorbimento dei metaboliti | |
| nl | Stoornis van metabolietabsorptie en transport | |
| pt | Alteração da absorção e transporte de metabólitos | |
| pl | Zaburzenia wchłaniania i transportu metabolitów | |
| cs | Poruchy absorpce a transportu metabolitů | |
| uk | Порушення всмоктування та транспорту метаболітів | |
| zh | 代谢物吸收-转运障碍 | |
| tr | Metabolit emilim ve taşınım bozuklukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017757 | E | validated | |
| MONDO | 17757 | E | validated | |
| UMLS | C5681033 | 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:68367Rare inborn error of metabolism
rare inborn errors of metabolism; 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/309824
- This record as JSON: /data/d/309824.json