ORPHA:89826
Rare skin disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 | Rare skin disease | |
| fr | Maladie rare de la peau | |
| de | Hautkrankheit, seltene | |
| es | Enfermedad cutánea rara | |
| it | Malattia cutanea rara | |
| nl | Zeldzame huidziekte | |
| pt | Doença de pele rara | |
| pl | Rzadkie choroby skóry | |
| cs | Vzácné kožní nemoci | |
| uk | Рідкісне шкірне захворювання | |
| zh | 罕见皮肤病 | |
| tr | Nadir cilt hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19519 | E | validated | |
| UMLS | C5681445 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Children (17):
- ORPHA:315350Autoimmune disease with skin involvement
- ORPHA:79377Dermis disorder
- ORPHA:79362Epidermal appendage anomaly
- ORPHA:79353Epidermal disease
- ORPHA:79391Immune deficiency with skin involvement
- ORPHA:79387Metabolic disease with skin involvement
- ORPHA:90077Other acquired skin disease
- ORPHA:79374Pigmentation anomaly of the skin
- ORPHA:79389Premature aging
- ORPHA:77240Primary lymphedema
- ORPHA:79390Rare photodermatosis
- ORPHA:79386Rare skin tumor or hamartoma
- ORPHA:79384Rare urticaria
- ORPHA:79382Subcutaneous tissue disease
- ORPHA:290836Systemic disease with skin involvement
- ORPHA:293815Toxic dermatosis
- ORPHA:79385Unclassified genetic skin disorder
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/89826
- This record as JSON: /data/d/89826.json