| HEMOCHROMATOSIS, TYPE 4 | |
| HEMOCHROMATOSIS DUE TO DEFECT IN FERROPORTIN | |
|
606069
OMIM = Online Mendelian Inheritance of Men | |
|
139491 | |
| Solute carrier family 40 member 1 | |
| rare autosomal dominant | |
| Laboratory findings | Ferritin inc (serum) |
| Symptoms | anemia arthritis cardiac arrhythmia, dysrhythmia cardiomyopathy cataract cirrhosis or fibrosis of liver fatigue, severe or unusual fever Glucose tolerance, impaired hyperpigmentation liver involvement or dysfunction pain, bones or joints |