Hemosiderosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An iron metabolism disease that has_material_basis_in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload. (Human Disease Ontology, DOID_12119)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006486
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Genes

1 genes/proteins associated with the disease Hemosiderosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ACO2 aconitase 2, mitochondrial 1.06808