ORPHA:901
Wells syndrome
Synonyms: Eosinophilic cellulitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Wells syndrome is characterised by the presence of recurrent cellulitis-like eruptions with eosinophilia.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Wells syndrome | Eosinophilic cellulitis |
| fr | Syndrome de Wells | Cellulite à éosinophiles |
| de | Wells-Syndrom | Zellulitis, eosinophile |
| es | Síndrome de Wells | |
| it | Sindrome di Wells | Cellulite da eosinofili |
| nl | Syndroom van Wells | Eosinofiele cellulitis |
| pt | Síndrome Wells | Celulite eosinofílica |
| pl | Zespół Wellsa | Eozynofilowe zapalenie tkanki łącznej |
| cs | Wellsův syndrom | Eosinofilní celulitida |
| uk | Синдром Веллса | Еозинофільний целюліт |
| zh | 韦尔斯综合征 | 嗜酸性蜂窝织炎 |
| tr | Wells sendromu | Eozinofilik selülit |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.3 | E | specific | validated |
| ICD-11 | EB30 | E | specific | validated |
| MONDO | 0019547 | E | validated | |
| MeSH | C536693 | E | validated | |
| UMLS | C0343101 | E | validated | |
| GARD | 329 | E | validated | |
| MedDRA | 10053776 | 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:90077Other acquired skin disease
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 |
|---|---|---|---|---|---|---|
| Cases/families | 200 cases | Worldwide | Case(s) | Validated | 23730155[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_23730155[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
9 annotations · validated 2016-07-15| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0100658 | Cellulitis | |
| HP:0000989 | Pruritus | |
| Frequent (79-30%) | ||
| HP:0008066 | Abnormal blistering of the skin | |
| HP:0000969 | Edema | |
| HP:0001880 | Increased total eosinophil count | |
| HP:0200037 | Skin vesicle | |
| Occasional (29-5%) | ||
| HP:0002829 | Arthralgia | |
| HP:0001945 | Fever | |
| Excluded (0%) | ||
| HP:0002633 | Vasculitis | |
Run the differential on the 2 obligate / very frequent terms
Annotation source: 25846461[PMID]_27357601[PMID]
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/901
- This record as JSON: /data/d/901.json