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Disease Hemochromatosis, type 3

Name Hemochromatosis, type 3
Synonyms Hemochromatosis due to defect in transferrin receptor 2 | HFE3
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C537248
OMIM® ID 604250
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes Hemochromatosis Has associated chemicals Has associated genes Hemochromatosis, type 3 Has associated chemicals Has associated genes
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Iron Metabolism Disorders Has associated chemicals Has associated genes Iron Overload Has associated chemicals Has associated genes Hemochromatosis Has associated chemicals Has associated genes Hemochromatosis, type 3 Has associated chemicals Has associated genes
3. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes Hemochromatosis Has associated chemicals Has associated genes Hemochromatosis, type 3 Has associated chemicals Has associated genes

Top ↑ Descendants

None.