Wells syndrome
General Information (adopted from Orphanet):
Synonyms, Signs: |
Eosinophilic cellulitis |
Number of Symptoms | 10 |
OrphanetNr: | 901 |
OMIM Id: |
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ICD-10: |
L98.3 |
UMLs: |
C0343101 |
MeSH: |
C536693 |
MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | 80 cases [Orphanet] |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Other acquired skin disease
-Rare skin disease |
Symptom Information:
|
(HPO:0001031) | Subcutaneous lipoma | Very frequent [Orphanet] | 112 / 7739 | |||
|
(HPO:0000989) | Pruritus | Very frequent [Orphanet] | 111 / 7739 | |||
|
(HPO:0010783) | Erythema | Frequent [Orphanet] | 138 / 7739 | |||
|
(HPO:0000988) | Skin rash | Very frequent [Orphanet] | 98 / 7739 | |||
|
(HPO:0200037) | Skin vesicle | Frequent [Orphanet] | 102 / 7739 | |||
|
(HPO:0001025) | Urticaria | Frequent [Orphanet] | 73 / 7739 | |||
|
(HPO:0001879) | Abnormality of eosinophils | Very frequent [Orphanet] | 20 / 7739 | |||
|
(HPO:0000969) | Edema | Very frequent [Orphanet] | 117 / 7739 | |||
|
(HPO:0003549) | Abnormality of connective tissue | Very frequent [Orphanet] | 22 / 7739 | |||
|
(HPO:0030350) | Erythematous papule | Frequent [Orphanet] | 123 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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