Bullous pemphigoid

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 11
OrphanetNr: 703
OMIM Id:
ICD-10: L12.0
UMLs: C0030805
MeSH: D010391
MedDRA:
Snomed: 77090002

Prevalence, inheritance and age of onset:

Prevalence: 2.5 of 100 000 [Orphanet]
Inheritance:
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Autoimmune bullous skin disease
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0011830) Abnormality of oral mucosa Very frequent [Orphanet] 47 / 7739
2
 (HPO:0000819) Diabetes mellitus Very frequent [Orphanet] 131 / 7739
3
 (HPO:0004325) Decreased body weight Very frequent [Orphanet] 492 / 7739
4
 (HPO:0010783) Erythema Very frequent [Orphanet] 138 / 7739
5
 (HPO:0200037) Skin vesicle Very frequent [Orphanet] 102 / 7739
6
 (HPO:0001025) Urticaria Very frequent [Orphanet] 73 / 7739
7
 (HPO:0000964) Eczema Very frequent [Orphanet] 81 / 7739
8
 (HPO:0003765) Psoriasis Frequent [Orphanet] 17 / 7739
9
 (HPO:0002960) Autoimmunity Very frequent [Orphanet] 78 / 7739
10
 (HPO:0010978) Abnormality of immune system physiology Very frequent [Orphanet] 148 / 7739
11
 (MedDRA:10025421) Macule Very frequent [Orphanet] 55 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: