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Hfe Hereditary Hemochromatosis
HFE hereditary hemochromatosis
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Hepatology
(10)
Hepcidin
Neonatal hemochromatosis
Primary biliary cirrhosis
Cirrhosis
Hepatocellular carcinoma
Hepatocellular carcinoma
Liver transplantation
Aceruloplasminemia
Liver disease
Alcoholic liver disease
Hepatomegaly
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Hematology
(8)
Transferrin saturation
Ferroportin
African iron overload
Iron homeostasis
Venipuncture
Venipuncture
Iron deficiency (medicine)
Blood transfusion
Hepcidin
more...
Gastroenterology
Iron overload
Nonalcoholic Steatohepatitis
Primary biliary cirrhosis
Cirrhosis
Liver transplantation
Genetic disorders
Compound heterozygotes
Otospondyl- omegaepiphyseal dysplasia
X-linked sideroblastic anemia
Porphyria cutanea tarda
Neonatal hemochromatosis
African iron overload
Aceruloplasminemia
Iron metabolism
(30)
Ferritin
Hemojuvelin
Hephaestin
Juvenile hemochromatosis
Serum iron
Serum iron
Siderosis
Total iron binding capacity
Transferrin receptor
Transferrin receptor-2
Aceruloplasminemia
African iron overload
Atransferrinemia
Ceruloplasmin
Ferroportin
Haemochromatosis type 3
Hemoproteins
Hemosiderin
Hemosiderosis
Hepcidin
Iron deficiency (medicine)
Iron deficiency anemia
Iron homeostasis
Iron metabolism disorder
Iron overload
Iron tests
Iron-binding proteins
Neonatal hemochromatosis
TFRC
Transferrin
Transferrin saturation
more...
Blood tests
Ferritin
Serum iron
Venipuncture
Total iron binding capacity
Genetic genealogy
Haplotype
Allele
Genetic disorders
Genetics
(11)
Mutation
Penetrance
Genetic test
Cytogenetic
Molecular cytogenetics
Molecular cytogenetics
Hereditary
Polymorphism (biology)
Genotyping
Genotype
Genetic disorders
Compound heterozygotes
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Medical condition
(16)
Cardiac failure
Cardiomyopathy
Storage disease
Hypogonadism
Iron overload
Iron overload
Neonatal hemochromatosis
Primary biliary cirrhosis
African iron overload
Cirrhosis
X-linked sideroblastic anemia
Hepatocellular carcinoma
Porphyria cutanea tarda
Fibrogenesis
Aceruloplasminemia
Siderosis
Nonalcoholic Steatohepatitis
more...
See also
(20)
Diseases and disorders
Symptoms
HFE (gene)
Cell metabolism
DMT1
DMT1
Liver biopsy
Homozygotes
Genetic screening
Homozygous
HAMP
Neuronopathy
Genetic counselor
Fibrogenesis
Hepatic
The mutation
Stellate cells
Ann Intern Med
Northern European
Enterocyte
Hispanic Health Council
more...
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