ORPHA:79183
Disorder of ketolysis
- 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 ketolysis | |
| fr | Trouble de la cétolyse | |
| de | Ketokörper-Stoffwechselstörung | |
| es | Trastornos del metabolismo de los cuerpos cetónicos | |
| it | Difetto del metabolismo dei corpi chetonici | |
| nl | Stoornis van ketolyse | |
| pt | Doença de cetólise | |
| pl | Zaburzenie metabolizmu ciał ketonowych | |
| cs | Porucha ketolýzy | |
| uk | Порушення кетолізу | |
| zh | 解酮作用异常 | |
| tr | Ketoliz bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C52.02 | E | specific | validated |
| MONDO | 0019229 | E | validated | |
| MONDO | 19229 | E | validated | |
| UMLS | C5681845 | 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:79174Disorder of fatty acid oxidation and ketone body 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79183
- This record as JSON: /data/d/79183.json