ORPHA:46485
Superficial pemphigus
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- All ages
- 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 | Superficial pemphigus | |
| fr | Pemphigus superficiel | |
| de | Pemphigus superficial | |
| es | Pénfigo superficial | |
| it | Pemfigo superficiale | |
| nl | Superficiële pemfigus | Pemphigus superficialis |
| pt | Pênfigo superficial | |
| pl | Pęcherzyca powierzchowna | |
| cs | Povrchový pemphigus | |
| uk | Поверхневий пемфігус | |
| zh | 表皮类天疱疮 | |
| tr | Yüzeyel pemfigus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18745 | E | validated | |
| UMLS | C5681323 | 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:79669Autoimmune bullous skin disease
rare skin diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 1.2 / 100 000 | Europe | Value and class | Validated | [EXPERT] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/46485
- This record as JSON: /data/d/46485.json