|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes associated with the disease juvenile hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.