Pyoderma gangrenosum
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 8 |
| OrphanetNr: | 48104 |
| OMIM Id: |
|
| ICD-10: |
L88 |
| UMLs: |
C0085652 |
| MeSH: |
D017511 |
| MedDRA: |
10037635 |
| Snomed: |
74578003 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Unknown [Orphanet] |
| Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Other acquired skin disease
-Rare skin disease Pyogenic autoinflammatory syndrome -Rare systemic or rheumatologic disease |
Symptom Information:
|
|
(HPO:0010783) | Erythema | Occasional [Orphanet] | 138 / 7739 | |||
|
|
(HPO:0200037) | Skin vesicle | Frequent [Orphanet] | 102 / 7739 | |||
|
|
(HPO:0001031) | Subcutaneous lipoma | Occasional [Orphanet] | 112 / 7739 | |||
|
|
(HPO:0200042) | Skin ulcer | Very frequent [Orphanet] | 138 / 7739 | |||
|
|
(HPO:0000988) | Skin rash | Very frequent [Orphanet] | 98 / 7739 | |||
|
|
(HPO:0002113) | Pulmonary infiltrates | Very frequent [Orphanet] | 36 / 7739 | |||
|
|
(HPO:0100614) | Myositis | Very frequent [Orphanet] | 21 / 7739 | |||
|
|
(OMIM) | Stiff skin | Frequent [Orphanet] | 31 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|