| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
