ORPHA:79188
Peroxisomal beta-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 | Peroxisomal beta-oxidation disorder | |
| fr | Anomalie de la bêta-oxydation péroxysomale | |
| de | Peroxisomale beta-Oxidationsstörung | |
| es | Enfermedad de la beta oxidación peroxisomal | |
| it | Malattia della beta-ossidazione perossisomiale | |
| nl | Stoornis van peroxisomale bèta-oxidatie | |
| pt | Doença da beta-oxidação peroxissomal | |
| pl | Zaburzenie beta-oksydacji peroksysomalnej | |
| cs | Porucha peroxisomální beta oxidace | |
| uk | Порушення пероксисомного бета-окислення | |
| zh | 过氧化物酶体β氧化异常 | |
| tr | Peroksizomal beta oksidasyonu bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019233 | E | validated | |
| MONDO | 19233 | E | validated | |
| UMLS | C5681280 | E | validated | |
| GARD | 12470 | 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:309810Disorder of peroxisomal alpha-, beta- and omega-oxidation
rare inborn errors of metabolism; rare genetic diseases; rare transplant-related disorders
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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.
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/79188
- This record as JSON: /data/d/79188.json