| HEMOCHROMATOSIS, TYPE 5 | |
|
615517
OMIM = Online Mendelian Inheritance of Men | |
|
247790 | |
| Ferritin heavy chain | |
| 1.16.3.1 | |
| rare autosomal dominant mutation in the FTH1 gene | |
| Laboratory findings | Ferritin inc (serum) Iron inc (serum) |
| Symptoms | no clinical symptoms (probably) |