ORPHA:309827
Disorder of vitamin and non-protein cofactor 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 vitamin and non-protein cofactor absorption and transport | |
| fr | Anomalie d'absorption et de transport des vitamines et cofacteurs non protéiques | |
| de | Vitamin- und nicht-Protein Kofaktor-Stoffwechsel- und Transportstörungen | |
| es | Trastornos de absorción y transporte de vitaminas y del cofactor no protéico | |
| it | Difetto del trasporto e dell'assorbimento delle vitamine e del cofattore non proteico | |
| nl | Stoornis van vitamine en niet-eiwit cofactorabsorptie en transport | |
| pt | Alteração da absorção e transporte de co-fatores de vitaminas e não proteínas | |
| pl | Zaburzenia wchłaniania i transportu witamin i niebiałkowych kofaktorów | |
| cs | Porucha absorpce a transportu vitaminů a nebílkovinných kofaktorů | |
| uk | Порушення всмоктування та транспорту вітамінів і небілкових кофакторів | |
| zh | 维生素和非蛋白质辅因子吸收-转运障碍 | |
| tr | Vitamin ve protein dışı kofaktör emilim ve taşınım bozuklukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C63 | E | specific | validated |
| MONDO | 0017758 | E | validated | |
| MONDO | 17758 | E | validated | |
| UMLS | C5681037 | 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:309824Disorder of metabolite absorption and transport
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.
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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/309827
- This record as JSON: /data/d/309827.json