|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Type 3 hemochromatosis is a 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_225123)|
|Downloads & Tools|
1 genes associated with the hemochromatosis, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
|TFR2||transferrin receptor 2|