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Sarcoidosis
3 OMIM references -
2 associated genes
20 connected diseases
No signs/symptoms info
Disease Type of connection
Bullous pemphigoid
Diffuse cutaneous systemic sclerosis
Follicular lymphoma
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
Narcolepsy without cataplexy
Narcolepsy-cataplexy
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):
- Besnier-Boeck-Schaumann disease
- Boeck sarcoid
- Boeck's sarcoid
Classification (Orphanet):
- Rare cardiac disease
- Rare endocrine disease
- Rare eye disease
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
3 OMIM references -
1 MeSH reference: D012507
Gene symbol UniProt reference OMIM reference
BTNL2 Q9UIR0606000
HLA-DRB1 P04229142857
No signs/symptoms info available.