ORPHA:183426
Genetic epidermal disorder
- 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 | Genetic epidermal disorder | |
| fr | Maladie génétique de l'épiderme | |
| de | Epidermale Krankheit, genetisch bedingte | |
| es | Enfermedad genética de la epidermis | |
| it | Malattia genetica dell'epidermide | |
| nl | Genetische epidermale aandoening | |
| pt | Doença epidérmica genética | |
| pl | Genetyczna choroba naskórka | |
| cs | Geneticky podmíněné poruchy epidermis | |
| uk | Генетично обумовленне епідермальне захворювання | |
| zh | 遗传性表皮疾病 | |
| tr | Genetik epidermal bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15946 | E | validated | |
| UMLS | C5680588 | 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:68346Rare genetic skin disease
rare genetic diseases
Children (11):
- ORPHA:183441Genetic acrokeratoderma
- ORPHA:183438Genetic erythrokeratoderma
- ORPHA:183444Genetic porokeratosis
- ORPHA:2841Hailey-Hailey disease
- ORPHA:79357Hereditary palmoplantar keratoderma
- ORPHA:222628Hereditary poikiloderma
- ORPHA:79361Inherited epidermolysis bullosa
- ORPHA:183435Inherited ichthyosis
- ORPHA:488168Microcephaly-congenital cataract-psoriasiform dermatitis syndrome
- ORPHA:79360Other genetic epidermal disease
- ORPHA:168606Seborrhea-like dermatitis with psoriasiform elements
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/183426
- This record as JSON: /data/d/183426.json