Disease #03983 (HFE5 (hemochromatosis, type 5 (HFE-5)), OMIM:615517)

Official abbreviation HFE5
Name hemochromatosis, type 5 (HFE-5)
OMIM ID 615517
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene FTH1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00088255 - PubMed: Kato 2001, Journal: Kato 2001 3-generation family, 4 affecteds (3F, M) F;M no Japan - - - - - HFE5 Female patient (56y) admitted to hospital for examination of early gastric cancer. Hepatic CT: 92 units. T2-weighted MRI showed low intensity signal of liver, heart and bone marrow. Serum ferritin 1,654 μg/l; serum Fe 156 μg/dl; transferrin saturation 58%; TIBC 269 μg/dl. Histology of liver biopsy showed heavy iron deposition in most hepatocytes and some Kupffer cells. Histology of splenectomy specimen showed gross iron deposition in macrophages. Hepatic iron concentration was not measured and venesection was not performed. FTH1, HFE, TFR2 FTH1 1 1 Johan den Dunnen
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