ORPHA:308459
Disorder of glycolysis
- 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 glycolysis | |
| fr | Trouble de la glycolyse | |
| de | Störung der Glykolyse | |
| es | Alteraciones de la glucólisis | |
| it | Difetto della glicolisi | |
| nl | Stoornis van glycolyse | |
| pt | Alteração da glicólise | |
| pl | Zaburzenia glikolizy | |
| cs | Poruchy glykolýzy | |
| uk | Порушення гліколізу | |
| zh | 糖酵解紊乱 | |
| tr | Glikoliz bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017688 | E | validated | |
| MONDO | 17688 | E | validated | |
| UMLS | C5681073 | 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
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/308459
- This record as JSON: /data/d/308459.json