ORPHA:290836
Systemic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Systemic disease with skin involvement | |
| fr | Maladie systémique avec atteinte cutanée | |
| de | Systemische Krankheit mit Hautbeteiligung | |
| es | Enfermedad sistémica con afectación de la piel | |
| it | Malattia sistemica con coinvolgimento cutaneo | |
| nl | Systemische aandoening met betrokkenheid van huid | |
| pt | Doença sistémica com envolvimento da pele | |
| pl | Choroba układowa z udziałem skóry | |
| cs | Systémová onemocnění s postižením kůže | |
| uk | Системне захворювання з ураженням шкіри | |
| zh | 累及皮肤的全身性疾病 | |
| tr | Deri tutulumu ile seyreden sistemik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17368 | E | validated | |
| UMLS | C5681006 | 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 (1):
- ORPHA:89826Rare skin disease
rare skin diseases
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/290836
- This record as JSON: /data/d/290836.json