| MP term: | hemochromatosis |
| MP id: | MP:0005638 |
| Definition: | disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary |
| Number of paths to term: | 3 |
denotes an 'is-a' relationship
denotes a 'part-of' relationship
homeostasis/metabolism phenotypeabnormal homeostasisabnormal ion homeostasisabnormal iron homeostasisabnormal iron levelabnormal brain iron levelabnormal circulating iron level +abnormal heart iron levelabnormal intestinal iron levelabnormal kidney iron level +abnormal liver iron level +abnormal spleen iron level +hemochromatosis [MP:0005638] (18 genotypes, 18 annotations)hemosiderosishomeostasis/metabolism phenotypeabnormal homeostasisabnormal mineral homeostasisabnormal iron homeostasisabnormal iron levelabnormal brain iron levelabnormal circulating iron level +abnormal heart iron levelabnormal intestinal iron levelabnormal kidney iron level +abnormal liver iron level +abnormal spleen iron level +hemochromatosis [MP:0005638] (18 genotypes, 18 annotations)hemosiderosishomeostasis/metabolism phenotypeabnormal homeostasisabnormal mineral homeostasisabnormal mineral levelabnormal iron levelabnormal brain iron levelabnormal circulating iron level +abnormal heart iron levelabnormal intestinal iron levelabnormal kidney iron level +abnormal liver iron level +abnormal spleen iron level +hemochromatosis [MP:0005638] (18 genotypes, 18 annotations)hemosiderosisMouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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