Pemphigoid gestationis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 4 |
| OrphanetNr: | 63275 |
| OMIM Id: |
|
| ICD-10: |
L12.8 |
| UMLs: |
C0019343 |
| MeSH: |
D006559 |
| MedDRA: |
10019939 |
| Snomed: |
86081009 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
|
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Autoimmune bullous skin disease
-Rare skin disease |
Symptom Information:
|
|
(HPO:0001622) | Premature birth | Very frequent [Orphanet] | 100 / 7739 | |||
|
|
(HPO:0004325) | Decreased body weight | Frequent [Orphanet] | 492 / 7739 | |||
|
|
(HPO:0001025) | Urticaria | Occasional [Orphanet] | 73 / 7739 | |||
|
|
(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|