ORPHA:309001
Disorder of carbohydrate 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 carbohydrate absorption and transport | |
| fr | Trouble du transport et de l'absorption des carbohydrates | |
| de | Störung der Kohlenhydrataufnahme und Transport | |
| es | Trastornos de absorción y transporte de los hidratos de carbono | |
| it | Difetto dell'assorbimento e del trasporto dei carboidrati | |
| nl | Stoornis van koolhydraatabsorptie en transport | |
| pt | Alteração da absorção e transporte de carboidratos | |
| pl | Zaburzenia wchłaniania i transportu węglowodorów | |
| cs | Poruchy absorpce a transportu cukrů | |
| uk | Порушення всмоктування та транспортування вуглеводів | |
| zh | 碳水化合物吸收和转运障碍 | |
| tr | Karbonhidrat emilimi ve taşınmasında bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C61 | E | specific | validated |
| MONDO | 0017706 | E | validated | |
| MONDO | 17706 | E | validated | |
| UMLS | C5681069 | 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:79161Disorder of carbohydrate metabolism
rare inborn errors of metabolism; rare genetic diseases
Children (8):
- ORPHA:103907Chronic diarrhea due to glucoamylase deficiency
- ORPHA:53690Congenital lactase deficiency
- ORPHA:35122Congenital sucrase-isomaltase deficiency
- ORPHA:165991Exercise-induced hyperinsulinism
- ORPHA:79178Glucose transport disorder
- ORPHA:469Hereditary fructose intolerance
- ORPHA:247794Juvenile cataract-microcornea-renal glucosuria syndrome
- ORPHA:103909Trehalase deficiency
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/309001
- This record as JSON: /data/d/309001.json