HFE-related hereditary haemochromatosis, Type 1 (Q97530): Difference between revisions
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A hemocromatose tipo 1 (clássica) é a forma mais comum de hemocromatose hereditária, um grupo de doenças caracterizado por deposição excessiva de ferro nos tecidos. A hemocromatose tipo 1 causa fadiga crônica, pigmentação bronzeada da pele e lesões nos tecidos do fígado, pâncreas, articulações, osso, glândulas endócrinas, coração, que resultam em várias complicações na idade adulta, incluindo fibrose hepática (cirrose com risco de carcinoma hepatocelular), diabetes mellitus, artropatia, osteoporose, hipogonadismo hipogonadotrópico e insuficiência cardíaca. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/108432760 / rank | |||||||||||||||
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CID11:ID_108432760 | |||||||||||||||
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dki-india-ID_108432760 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest 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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dki-india-ID_108432760
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Concluído
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15 August 2026
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