ORPHA:309115
Disorder of fatty acid oxidation and ketogenesis
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disorder of fatty acid oxidation and ketogenesis | |
| fr | Trouble de l'oxydation des acides gras et de la cétogenèse | |
| de | Störung der Fettsäureoxidation und Ketogenese | |
| es | Trastorno de la oxidación de ácidos grasos y de la cetogénesis | |
| it | Difetto di ossidazione degli acidi grassi e della chetogenesi | |
| nl | Stoornis van vetzuuroxidatie en ketogenese | |
| pt | Alteração da oxidação do ácido goedo mitocondrial | |
| pl | Zaburzenia oksydacji kwasów tłuszczowych i ketogenezy | |
| cs | Poruchy oxidace mastných kyselin a ketogeneze | |
| uk | Порушення окислення жирних кислот і кетогенезу | |
| zh | 脂肪酸氧化与生酮障碍 | |
| tr | Yağ asidi oksidasyonu ve ketogenez bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C52.01 | E | specific | validated |
| MONDO | 0017713 | E | validated | |
| MONDO | 17713 | E | validated | |
| UMLS | C5681071 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/309115
- This record as JSON: /data/d/309115.json