pseudoxanthoma elasticum Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disease characterized by the accumulation of deposits of calcium and other minerals in elastic fibers, which are a component of connective tissue, this can result in changes in the skin, eyes, cardiovascular system and gastrointestinal system. (Human Disease Ontology, DOID_2738)
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Genes

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

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
CAT catalase
CFH complement factor H
GPX1 glutathione peroxidase 1
ICAM1 intercellular adhesion molecule 1
SELE selectin E
SOD2 superoxide dismutase 2, mitochondrial