|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the hemochromatosis, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
|SLC40A1||solute carrier family 40 (iron-regulated transporter), member 1|