Dermatomyositis Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A myositis and is_a dermatitis that results_in inflammation located_in muscle and located_in skin. The disease may result from either a viral infection or an autoimmune reaction.|A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) (Experimental Factor Ontology, EFO_0000398)
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Genes

11 genes associated with the disease Dermatomyositis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
TSBP1 testis expressed basic protein 1 1.968
HLA-DRA major histocompatibility complex, class II, DR alpha 1.968
BTNL2 butyrophilin-like 2 1.968
HLA-DRB5 major histocompatibility complex, class II, DR beta 5 1.296
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 1.248
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1 1.248
HLA-DOA major histocompatibility complex, class II, DO alpha 1.248
COL11A2 collagen, type XI, alpha 2 1.248
BRD2 bromodomain containing 2 1.248
LRRC18 leucine rich repeat containing 18 1.129
WDFY4 WDFY family member 4 1.129