ORPHA:97230
Solar urticaria
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare photodermatosis characterized by an abrupt onset of transient erythema, wheals, and pruritus appearing within minutes of exposure to light.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Solar urticaria | |
| fr | Urticaire solaire | |
| de | Licht-Urtikaria | Sonnenurtikaria · Urtikaria, solare |
| es | Urticaria solar | SU |
| it | Orticaria solare | |
| nl | Zonne-urticaria | Netelroos door zonnestraling · Urticaria door zonnestraling · Urticaria solaris |
| pt | Urticária solar | |
| pl | Pokrzywka słoneczna | |
| cs | Sluneční kopřivka | |
| uk | Сонячна кропивянка | |
| zh | 日光性蕁麻疹 | |
| tr | Güneş ürtikeri |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L56.3 | E | specific | validated |
| ICD-11 | EB01.Y | NTBT | index | validated |
| MONDO | 0019945 | E | validated | |
| MeSH | D000092130 | E | validated | |
| UMLS | C0263610 | E | validated | |
| MedDRA | 10041307 | 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:79390Rare photodermatosis
rare skin diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 3.1 / 100 000 | United Kingdom | Value and class | Validated | 12975156[PMID]_[EXPERT] |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_30585308[PMID]_27793344[PMID]_[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.
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HPO phenotypes
16 annotations · validated 2017-03-17| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000159 | Abnormal lip morphology | |
| HP:0030809 | Abnormal tongue morphology | |
| HP:0100665 | Angioedema | |
| HP:0000969 | Edema | |
| HP:0002315 | Headache | |
| HP:0100326 | Immunologic hypersensitivity | |
| HP:0002018 | Nausea | |
| HP:0100539 | Periorbital edema | |
| HP:0000989 | Pruritus | |
| HP:0001279 | Syncope | |
| HP:0001025 | Urticaria | |
| HP:0002321 | Vertigo | |
| HP:0030828 | Wheezing | |
| Frequent (79-30%) | ||
| HP:0002094 | Dyspnea | |
| Occasional (29-5%) | ||
| HP:0011971 | Dermatographic urticaria | |
| Very rare (<4-1%) | ||
| HP:0100845 | Anaphylactic shock | |
Run the differential on the 12 obligate / very frequent terms
Annotation source: 19022098[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/97230
- This record as JSON: /data/d/97230.json