ORPHA:309816
Disorder of bilirubin metabolism and excretion
- 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 bilirubin metabolism and excretion | |
| fr | Trouble du métabolisme et de l'excrétion de la bilirubine | |
| de | Bilirubin-Stoffwechselstörung | |
| es | Trastornos del metabolismo y la excreción de la bilirrubina | |
| it | Difetto del metabolismo e dell'escrezione di bilirubina | |
| nl | Stoornis van bilirubinemetabolisme en -excretie | |
| pt | Alteração do metabolismo e excreção de bilirrubina | |
| pl | Zaburzenia metabolizmu i wydzielania bilirubiny | |
| cs | Poruchy metabolismu a exkrece bilirubinu | |
| uk | Порушення обміну та виведення білірубіну | |
| zh | 胆红素代谢排泄障碍 | |
| tr | Bilirubin metabolizması ve atılım bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C58.0 | E | specific | validated |
| MONDO | 0017755 | E | validated | |
| MONDO | 17755 | E | validated | |
| UMLS | C0349427 | 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:309813Disorder of porphyrin and heme metabolism
rare inborn errors of metabolism; rare genetic diseases
Children (7):
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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/309816
- This record as JSON: /data/d/309816.json