ORPHA:79177
Gluconeogenesis disorder
- 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 | Gluconeogenesis disorder | |
| fr | Trouble de la gluconéogenèse | Trouble de la néoglucogenèse |
| de | Glukoneogenese-Störung | |
| es | Enfermedad de la gluconeogénesis | |
| it | Malattia della gluconeogenesi | |
| nl | Stoornis van gluconeogenese | |
| pt | Doença da gluconeogénese | |
| pl | Zaburzenie glukoneogenezy | |
| cs | Poruchy glukoneogeneze | |
| uk | Порушення глюконеогенезу | |
| zh | 糖异生异常 | |
| tr | Glukoneogenez bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019225 | E | validated | |
| MONDO | 19225 | E | validated | |
| UMLS | C1398833 | 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/79177
- This record as JSON: /data/d/79177.json