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Bullous pemphigoid
2 associated genes
20 connected diseases
12 signs/symptoms
Disease Type of connection
Narcolepsy without cataplexy
Narcolepsy-cataplexy
Diffuse cutaneous systemic sclerosis
Follicular lymphoma
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
Sarcoidosis
Graham Little-Piccardi-Lassueur syndrome
17p13.3 microduplication syndrome
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Common variable immunodeficiency
Distal 17p13.3 microdeletion syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Miller-Dieker syndrome
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Precursor T-cell acute lymphoblastic leukemia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare skin disease
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D010391
Gene symbol UniProt reference OMIM reference
HLA-DQB1 P01920604305
HLA-DRB1 P04229142857
Very frequent
- Autoimmunity / autoimmune reaction / autoantibodies
- Diabetes mellitus
- Eczema
- Enanthema / aphtosa / aphta / leukoplakia
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Immunodeficiency / increased susceptibility to infections / recurrent infections
- Macules
- Negative Nikolski's sign
- Urticaria
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment
- Weight loss / loss of appetite / break in weight curve / general health alteration

Frequent
- Psoriasis