ORPHA:79390
Rare photodermatosis
Synonyms: Rare skin photosensitivity
- 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 | Rare photodermatosis | Rare skin photosensitivity |
| fr | Photodermatose rare | Photosensitibilité cutanée rare |
| de | Photodermatose, seltene | Photosensitivität der Haut |
| es | Fotodermatosis rara | Fotosensibilidad cutánea rara |
| it | Fotodermatosi rara | Fotosensibilità cutanea rara |
| nl | Zeldzame fotodermatose | Zeldzame fotosensitiviteit van huid · Zeldzame lichtgevoeligheid van huid |
| pt | Fotodermatose rara | Fotossensibilidade dcutânea rara |
| pl | Rzadka fotodermatoza | Rzadka wrażliwość skóry na światło |
| cs | Vzácné fotodermatózy | Vzácná kožní fotosenzitivita · Vzácná fotosenzitivita kůže |
| uk | Рідкісний фотодерматоз | Рідкісна світлочутливість шкіри |
| zh | 罕见日光性皮炎 | 罕见皮肤光敏感 |
| tr | Nadir fotodermatoz | Nadir cilt fotosensitivitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19304 | E | validated | |
| UMLS | C5680199 | 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:89826Rare skin disease
rare skin diseases
Children (13):
- ORPHA:330061Actinic prurigo
- ORPHA:125Bloom syndrome
- ORPHA:330064Chronic actinic dermatitis
- ORPHA:2116Hartnup disease
- ORPHA:330058Hydroa vacciniforme
- ORPHA:2908Kindler epidermolysis bullosa
- ORPHA:738Porphyria
- ORPHA:2909Rothmund-Thomson syndrome
- ORPHA:97230Solar urticaria
- 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/79390
- This record as JSON: /data/d/79390.json