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Limited systemic sclerosis
1 associated gene
20 connected diseases
No signs/symptoms info
Disease Type of connection
Bullous pemphigoid
Diffuse cutaneous systemic sclerosis
Follicular lymphoma
Limited cutaneous systemic sclerosis
Narcolepsy without cataplexy
Narcolepsy-cataplexy
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):
- Systemic sclerosis sine scleroderma
Classification (Orphanet):
- Rare cardiac disease
- Rare renal disease
- Rare respiratory disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
HLA-DRB1 P04229142857
No signs/symptoms info available.