Subcorneal pustular dermatosis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Subcorneal pustular dermatitis Sneddon-Wilkinson disease Pustulosis subcornealis |
| Number of Symptoms | 6 |
| OrphanetNr: | 48377 |
| OMIM Id: |
|
| ICD-10: |
L13.1 |
| UMLs: |
C0600336 |
| MeSH: |
|
| MedDRA: |
10042342 |
| Snomed: |
25147002 |
Prevalence, inheritance and age of onset:
| Prevalence: | 200 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:0000989) | Pruritus | Frequent [Orphanet] | 111 / 7739 | |||
|
|
(HPO:0200039) | Pustule | Very frequent [Orphanet] | 20 / 7739 | |||
|
|
(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
|
|
(HPO:0007400) | Irregular hyperpigmentation | Frequent [Orphanet] | 72 / 7739 | |||
|
|
(HPO:0006775) | Multiple myeloma | Occasional [Orphanet] | 10 / 7739 | |||
|
|
(HPO:0002960) | Autoimmunity | Occasional [Orphanet] | 78 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|