Hemochromatosis type 4 (Q28448698)
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hemochromatosis that has material basis in heterozygous mutation in the SLC40A1 gene on chromosome 2q32
- hemochromatosis type 4
- hemochromatosis due to defect in ferroportin
- HFE4
- ferroportin disease
- autosomal dominant hereditary hemochromatosis
- HEMOCHROMATOSIS, TYPE 4; HFE4
- HEMOCHROMATOSIS, TYPE 4
- Hemochromatosis Due to Defect 1N Ferroportin
- Hemochromatosis, Autosomal Dominant
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Hemochromatosis type 4 |
hemochromatosis that has material basis in heterozygous mutation in the SLC40A1 gene on chromosome 2q32 |
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Wikipedia(3 entries)
- arwiki داء ترسب الأصبغة الدموية من النوع 4
- bswiki Hemohromatoza tip 4
- enwiki Hemochromatosis type 4