ORPHA:717868
Rare skin disease with inflammatory bowel disease
- 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
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare skin disease with inflammatory bowel disease | |
| fr | Maladie rare de la peau avec maladie inflammatoire de l'intestin | |
| de | Seltene Hautkrankheit mit entzündlicher Darmerkrankung | |
| es | Enfermedad cutánea rara con enfermedad inflamatoria intestinal | |
| it | Malattia cutanea rara con malattia infiammatoria dell'intestino | |
| nl | Zeldzame huidziekte met inflammatoire darmziekte | |
| pt | Rare skin disease with inflammatory bowel disease | |
| pl | Rare skin disease with inflammatory bowel disease | |
| cs | Rare skin disease with inflammatory bowel disease |
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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:717862Rare disorder with inflammatory bowel disease
rare gastroenterological diseases; rare genetic diseases; rare transplant-related disorders
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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.
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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/717868
- This record as JSON: /data/d/717868.json