ORPHA:659698
Hepatic cutaneous porphyria
- Type
- Clinical group
- 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
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hepatic cutaneous porphyria | |
| fr | Porphyrie cutanée hépatique | |
| de | Hepatische kutane Porphyrie | |
| es | Porfiria hepática cutánea | |
| it | Porfiria cutanea epatica | |
| nl | Hepatische cutane porfyrie | |
| pt | Porfiria cutânea hepática | |
| pl | Porfiria wątrobowo-skórna | |
| cs | Jaterní kožní porfyrie | |
| uk | Печінкова шкірна порфірія |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:659694Hepatic porphyria
rare inborn errors of metabolism; rare genetic diseases; rare hepatic diseases; rare skin diseases; rare renal 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/659698
- This record as JSON: /data/d/659698.json