decreased serum ceruloplasmin Gene Set

Dataset HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0010837
Similar Terms
Downloads & Tools

Genes

1 genes associated with the decreased serum ceruloplasmin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1