hemochromatosis, type 4 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemochromatosis type 4 (also called ferroportin disease) 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_139491)
External Link http://www.omim.org/entry/606069
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1 genes associated with the hemochromatosis, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1