ORPHA:79161
Disorder of carbohydrate metabolism
- 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 metabolism | |
| fr | Trouble du métabolisme des hydrates de carbone | Anomalie du métabolisme des sucres |
| de | Kohlenhydrat-Stoffwechselstörung | |
| es | Enfermedad del metabolismo de los carbohidratos | |
| it | Malattia del metabolismo dei carboidrati | |
| nl | Stoornis van koolhydraatmetabolisme | |
| pt | Doença do metabolismo dos carbohidratos | |
| pl | Zaburzenie metabolizmu węglowodanów | |
| cs | Poruchy metabolismu sacharidů | |
| uk | Порушення вуглеводного обміну | |
| zh | 碳水化合物代谢紊乱 | |
| tr | Karbonhidrat metabolizması bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019214 | E | validated | |
| MONDO | 19214 | E | validated | |
| UMLS | C0149670 | E | validated | |
| MedDRA | 10061023 | 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:68367Rare inborn error of metabolism
rare inborn errors of metabolism; rare genetic diseases
Children (9):
- ORPHA:309001Disorder of carbohydrate absorption and transport
- ORPHA:308463Disorder of fructose metabolism
- ORPHA:308467Disorder of galactose metabolism
- ORPHA:79179Disorder of glycerol metabolism
- ORPHA:308459Disorder of glycolysis
- ORPHA:308998Disorder of glyoxylate metabolism
- ORPHA:440701Disorders of pentose/polyol metabolism
- ORPHA:79177Gluconeogenesis disorder
- ORPHA:79201Glycogen storage disease
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/79161
- This record as JSON: /data/d/79161.json