HFE-related hereditary haemochromatosis, Type 1 (Q97530): Difference between revisions
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Revision as of 13:38, 16 August 2026
Hemochromatosis type 1 (classic) is the most common form of hereditary hemochromatosis (HH), a group of diseases characterised by excessive tissue iron deposition. Hemochromatosis type 1 causes chronic fatigue, bronzed skin pigmentation and tissue damage in the liver, pancreas, joints, bone, endocrine glands, heart, which result in various complications in adulthood including liver fibrosis (cirrhosis with a risk of hepatocellular carcinoma), diabetes mellitus, arthropathy, osteoporosis, hypogonadotropic hypogonadism, and cardiac failure.
| Language | Label | Description | Also known as |
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| default for all languages | ID_108432760 |
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| English | HFE-related hereditary haemochromatosis, Type 1 |
Hemochromatosis type 1 (classic) is the most common form of hereditary hemochromatosis (HH), a group of diseases characterised by excessive tissue iron deposition. Hemochromatosis type 1 causes chronic fatigue, bronzed skin pigmentation and tissue damage in the liver, pancreas, joints, bone, endocrine glands, heart, which result in various complications in adulthood including liver fibrosis (cirrhosis with a risk of hepatocellular carcinoma), diabetes mellitus, arthropathy, osteoporosis, hypogonadotropic hypogonadism, and cardiac failure. |
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CID11:ID_108432760
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