ORPHA:315350
Autoimmune disease with skin involvement
- 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 | Autoimmune disease with skin involvement | |
| fr | Maladie auto-immune avec atteinte cutanée | |
| de | Autoimmune Krankheit mit Hautbeteiligung | |
| es | Enfermedad autoinmune con afectación de la piel | |
| it | Malattia autoimmune con coinvolgimento cutaneo | |
| nl | Auto-immuunziekte met betrokkenheid van huid | |
| pt | Doença autoimune com envolvimento da pele | |
| pl | Choroba autoimmunologiczna obejmująca skórę | |
| cs | Autoimunitní onemocnění s postižením kůže | |
| uk | Аутоімунне захворювання з ураженням шкіри | |
| zh | 自身免疫性疾病累及皮肤 | |
| tr | Deri tutulumu ile seyreden otoimmün hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17841 | E | validated | |
| UMLS | C5680965 | 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:89826Rare skin disease
rare skin diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:247871OBSOLETE: Vitiligo-associated autoimmune disease referred to · inactive
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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/315350
- This record as JSON: /data/d/315350.json