decreased serum ceruloplasmin Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A kind of Abnormality of copper homeostasis related to a decreased concentration of ceruloplasmin in the blood. (Human Phenotype Ontology, HP_0010837)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0010837
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Genes

1 genes associated with the decreased serum ceruloplasmin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CP ceruloplasmin (ferroxidase) 1.48419