hemochromatosis type 3 (Q3144936)
Jump to navigation
Jump to search
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22
- TFR2-related hemochromatosis
- HFE3
- hemochromatosis due to defect in transferrin receptor 2
- HEMOCHROMATOSIS, TYPE 3
- HEMOCHROMATOSIS, TYPE 3; HFE3
- Hemochromatosis Due to Defect 1N Transferrin Receptor 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hemochromatosis type 3 |
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22 |
|
Statements
2 references
1 reference
3 references
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(3 entries)
- arwiki داء ترسب الأصبغة الدموية من النمط 3
- enwiki Haemochromatosis type 3
- frwiki Hémochromatose par mutation TFR2