ORPHA:309133
Metabolic disease due to other fatty acid oxidation 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Metabolic disease due to other fatty acid oxidation disorder | |
| fr | Maladie métabolique par une autre anomalie de l'oxydation des acides gras | |
| de | Stoffwechselkrankheit durch Fettsäureoxidationsstörung | |
| es | Enfermedad metabólica por otro trastorno de la oxidación de ácidos grasos | |
| it | Malattia metabolica da difetto di ossidazione di altri acidi grassi | |
| nl | Stofwisselingsziekte door andere vetzuuroxidatiestoornis | |
| pt | Outro distúrbio de oxidação de ácidos gordos e metabolismo dos corpos cetónicos | |
| pl | Choroba metaboliczna spowodowana zaburzeniami innych kwasów tłuszczowych | |
| cs | Metabolická onemocnění způsobená jinými poruchami oxidace mastných kyselin | |
| uk | Метаболічні захворювання, спричинені іншими порушеннями окислення жирних кислот | |
| zh | 其他脂肪酸氧化紊乱所致代谢性疾病 | |
| tr | Diğer yağ asidi oksidasyon bozukluğuna bağlı metabolik hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17717 | E | validated | |
| UMLS | C5681079 | 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
Children (1):
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/309133
- This record as JSON: /data/d/309133.json