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| Term | hemochromatosis type 2 | ID (Ontology) | DOID:0111034 (Human Disease) |
| Definition | A hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis. | ||
| Also Known As | "HFE2" ; "JHH" ; "juvenile hemochromatosis" | ||
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metal metabolism disorder |__hemochromatosis |__hemochromatosis type 2 |__hemochromatosis type 2A |__hemochromatosis type 2B |
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| Is a | hemochromatosis | ||
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GARD:10092 ICD10CM:E83.1 MESH:C537247 ORDO:79230 |
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