ORPHA:79353
Epidermal 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Epidermal disease | |
| fr | Maladie de l'épiderme | |
| de | Epidermale Krankheit | |
| es | Enfermedad epidérmica | |
| it | Malattia epidermica | |
| nl | Epidermale aandoening | |
| pt | Doença epidérmica | |
| pl | Choroba naskórka | |
| cs | Nemoci postihující epidermis | |
| uk | Епідермальне захворювання | |
| zh | 表皮疾病 | |
| tr | Epidermal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019268 | E | validated | |
| MONDO | 19268 | E | validated | |
| UMLS | C5681492 | 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
Children (9):
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79353
- This record as JSON: /data/d/79353.json