|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormally reduced concentration of ferritin, a ubiquitous intracellular protein that stores iron, in the blood. (Human Phenotype Ontology, HP_0012343)|
|Downloads & Tools|
1 genes associated with the decreased serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|FTL||ferritin, light polypeptide|