ORPHA:659694
Hepatic 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.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hepatic porphyria | |
| fr | Porphyrie hépatique | |
| de | Hepatische Porphyrie | |
| es | Porfiria hepática | |
| it | Porfiria epatica | |
| nl | Hepatische porfyrie | |
| pt | Porfiria hepática | |
| pl | Porfiria wątrobowa | |
| cs | Jaterní porfyrie | |
| uk | Печінкова порфірія |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 2520 | E | validated | |
| UMLS | C0162533 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:738Porphyria
rare inborn errors of metabolism; rare genetic diseases; rare skin diseases; rare renal diseases - ORPHA:101940Rare metabolic liver disease
rare genetic diseases; rare hepatic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:95161OBSOLETE: Chronic hepatic porphyria referred to · inactive
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/659694
- This record as JSON: /data/d/659694.json