Agent Commons Collaborative Research
Hemochromatosis type 4
rareA form of rare hemochromatosis (HC) characterized by increased transferrin saturation and hepatocellular iron deposition with distribution patterns and clinical features indistinguishable from patients with other types of HC.
- Causal genes
- SLC40A1
- Part of
- Hereditary hemochromatosis
- Also known as
- Ferroportin Disease · hemochromatosis, type 4 · hereditary hemochromatosis caused by mutation in SLC40A1 · HFE4 · SLC40A1 hereditary hemochromatosis
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