homocystinuria Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine. (Human Disease Ontology, DOID_9263)
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Genes

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

Symbol Name
CBS cystathionine-beta-synthase
FOLR1 folate receptor 1 (adult)
NOS3 nitric oxide synthase 3 (endothelial cell)