ORPHA:183490
Genetic photodermatosis
Synonyms: Genetic skin photosensitivity · Photogenodermatosis
- 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 photodermatosis | Genetic skin photosensitivity · Photogenodermatosis |
| fr | Photodermatose génétique | Photogénodermatose · Photosensibilité cutanée génétique |
| de | Photodermatose, genetische | Photogenodermatose · Photosensitivität der Haut, genetisch bedingte |
| es | Fotodermatosis genética | Fotogenodermatosis · Fotosensibilidad cutánea genética |
| it | Fotodermatosi genetica | Fotogenodermatosi · Fotosensibilità cutanea genetica |
| nl | Genetische fotodermatose | Fotogenodermatose · Genetische fotogevoeligheid van de huid · Photogénodermatose |
| pt | Fotossensibilidade da pele genética | |
| pl | Fotodermatoza uwarunkowana genetycznie | Fotogenodermatoza · Fotowrażliwość skóry uwarunkowana genetycznie |
| cs | Geneticky podmíněné fotodermatózy | Fotosenzitivní genodermatóza · Geneticky podmíněná fotosenzitivita kůže |
| uk | Генетично обумовлений фотодерматоз | Генетична світлочутливість шкіри · Фотогенодерматоз · Фотогенодерматоз |
| zh | 遗传性光照性皮肤病 | 遗传性皮肤光过敏 |
| tr | Genetik fotodermatoz | Fotogenodermatoz · Fotogenodermatoz · Genetik cilt fotosensitivitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15951 | E | validated | |
| UMLS | C5679594 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:68346Rare genetic skin disease
rare genetic diseases
Children (9):
- ORPHA:125Bloom syndrome
- ORPHA:2116Hartnup disease
- ORPHA:2908Kindler epidermolysis bullosa
- ORPHA:738Porphyria
- ORPHA:2909Rothmund-Thomson syndrome
- ORPHA:178338UV-sensitive syndrome
- ORPHA:910Xeroderma pigmentosum
- ORPHA:90342Xeroderma pigmentosum variant
- ORPHA:220295Xeroderma pigmentosum-Cockayne syndrome complex
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/183490
- This record as JSON: /data/d/183490.json