scleroderma Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A rheumatic disease and collagen disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs. (Human Disease Ontology, DOID_419)
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Genes

6 genes associated with the disease scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
FBN1	fibrillin 1
HLA-DPB1	major histocompatibility complex, class II, DP beta 1
HLA-DQB1	major histocompatibility complex, class II, DQ beta 1
HLA-DRB1	major histocompatibility complex, class II, DR beta 1
SPARC	secreted protein, acidic, cysteine-rich (osteonectin)
TNF	tumor necrosis factor