hemochromatosis, type 3 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/604250
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1 genes associated with the hemochromatosis, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TFR2 transferrin receptor 2