| 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 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the hemochromatosis, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TFR2 | transferrin receptor 2 |
