(Q3144936)
English
hemochromatosis type 3
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
Statements
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Identifiers
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Sitelinks
Wikipedia(3 entries)
- arwiki داء ترسب الأصبغة الدموية من النمط 3
- enwiki Haemochromatosis type 3
- frwiki Hémochromatose par mutation TFR2