|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A kind of Abnormality of copper homeostasis related to a decreased concentration of ceruloplasmin in the blood. (Human Phenotype Ontology, HP_0010837)|
|Downloads & Tools|
1 genes associated with the decreased serum ceruloplasmin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SLC33A1||solute carrier family 33 (acetyl-CoA transporter), member 1|