juvenile hemochromatosis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hemochromatosis type 2 (juvenile) is the early-onset and most severe form of rare hereditary hemochromatosis (HH; see this term), a group of diseases characterized by excessive tissue iron deposition of genetic origin. (Orphanet Rare Disease Ontology, Orphanet_79230)
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2 genes associated with the disease juvenile hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
HFE hemochromatosis
TFR2 transferrin receptor 2