decreased serum ferritin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally reduced concentration of ferritin, a ubiquitous intracellular protein that stores iron, in the blood. (Human Phenotype Ontology, HP_0012343)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012343
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Genes

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

Symbol Name
FTL ferritin, light polypeptide