Erythroderma Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An inflammatory exfoliative dermatosis involving nearly all of the surface of the skin. Erythroderma develops suddenly. A patchy erythema may generalize and spread to affect most of the skin. Scaling may appear in 2-6 days and be accompanied by hot, red, dry skin, malaise, and fever. (Human Phenotype Ontology, HP_0001019)
External Link	https://www.disgenet.org/browser/0/1/0/C0748052
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Genes

10 genes associated with the disease Erythroderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ACE	angiotensin I converting enzyme
ANG	angiogenin, ribonuclease, RNase A family, 5
CD34	CD34 molecule
HLA-A	major histocompatibility complex, class I, A
HLA-E	major histocompatibility complex, class I, E
ICAM1	intercellular adhesion molecule 1
IL17A	interleukin 17A
IL37	interleukin 37
IVL	involucrin
TNF	tumor necrosis factor