Paraneoplastic pemphigus
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 2 |
| OrphanetNr: | 63455 |
| OMIM Id: |
|
| ICD-10: |
L10.8 |
| UMLs: |
C1112570 |
| MeSH: |
|
| MedDRA: |
10057056 |
| Snomed: |
|
Prevalence, inheritance and age of onset:
| Prevalence: | > 60 cases [Orphanet] |
| Inheritance: |
Not applicable [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Autoimmune bullous skin disease
-Rare skin disease |
Symptom Information:
|
|
(HPO:0011830) | Abnormality of oral mucosa | Very frequent [Orphanet] | 47 / 7739 | |||
|
|
(HPO:0200037) | Skin vesicle | Very frequent [Orphanet] | 102 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|