"Hemochromatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
| Descriptor ID |
D006432
|
| MeSH Number(s) |
C16.320.565.618.337 C18.452.565.500.480 C18.452.648.618.337
|
| Concept/Terms |
Hemochromatosis- Hemochromatosis
- Bronzed Cirrhosis
- Bronzed Cirrhoses
- Cirrhoses, Bronzed
- Cirrhosis, Bronzed
- Diabetes, Bronze
- Haemochromatosis
- Haemochromatoses
- Von Recklenhausen-Applebaum Disease
- Disease, Von Recklenhausen-Applebaum
- Diseases, Von Recklenhausen-Applebaum
- Recklenhausen-Applebaum Disease, Von
- Recklenhausen-Applebaum Diseases, Von
- Von Recklenhausen Applebaum Disease
- Von Recklenhausen-Applebaum Diseases
- Bronze Diabetes
- Iron Storage Disorder
- Disorder, Iron Storage
- Disorders, Iron Storage
- Iron Storage Disorders
- Storage Disorder, Iron
- Storage Disorders, Iron
- Pigmentary Cirrhosis
- Cirrhoses, Pigmentary
- Cirrhosis, Pigmentary
- Pigmentary Cirrhoses
- Troisier-Hanot-Chauffard Syndrome
- Syndrome, Troisier-Hanot-Chauffard
- Syndromes, Troisier-Hanot-Chauffard
- Troisier Hanot Chauffard Syndrome
- Troisier-Hanot-Chauffard Syndromes
- Hemochromatoses
- Hemochromatose
Familial Hemochromatosis- Familial Hemochromatosis
- Familial Hemochromatoses
- Hemochromatoses, Familial
- Hemochromatosis, Familial
- Primary Hemochromatosis
- Genetic Hemochromatosis
- Genetic Hemochromatoses
- Hemochromatoses, Genetic
- Hemochromatosis, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Hemochromatosis".
Below are MeSH descriptors whose meaning is more specific than "Hemochromatosis".
This graph shows the total number of publications written about "Hemochromatosis" by people in this website by year, and whether "Hemochromatosis" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 1 | 2 |
| 2009 | 1 | 1 | 2 |
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click here.
Below are the most recent publications written about "Hemochromatosis" by people in Profiles.
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Tsai A, Paltiel HJ, Sena LM, Kim HB, Fishman SJ, Alomari AI. Neonatal hemochromatosis and patent ductus venosus: clinical course and diagnostic pitfalls. Pediatr Radiol. 2009 Aug; 39(8):823-7.
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Gaspari R, Cavaliere F, Sollazzi L, Perilli V, Melchionda I, Agnes S, Gasbarrini A, Avolio AW. Molecular adsorbent recirculating system (Mars) in patients with primary nonfunction and other causes of graft dysfunction after liver transplantation in the era of extended criteria donor organs. Transplant Proc. 2009 Jan-Feb; 41(1):253-8.
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Breda L, Gardenghi S, Guy E, Rachmilewitz EA, Weizer-Stern O, Adamsky K, Amariglio N, Rechavi G, Giardina PJ, Grady RW, Rivella S. Exploring the role of hepcidin, an antimicrobial and iron regulatory peptide, in increased iron absorption in beta-thalassemia. Ann N Y Acad Sci. 2005; 1054:417-22.
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Walker NJ, Zurier RB. Liver abnormalities in rheumatic diseases. Clin Liver Dis. 2002 Nov; 6(4):933-46.
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Wood RJ. The "anemic" enterocyte in hereditary hemochromatosis: molecular insights into the control of intestinal iron absorption. Nutr Rev. 2002 May; 60(5 Pt 1):144-8.
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Waxman S, Eustace S, Hartnell GG. Myocardial involvement in primary hemochromatosis demonstrated by magnetic resonance imaging. Am Heart J. 1994 Nov; 128(5):1047-9.
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Raptopoulos V, Karellas A, Bernstein J, Reale FR, Constantinou C, Zawacki JK. Value of dual-energy CT in differentiating focal fatty infiltration of the liver from low-density masses. AJR Am J Roentgenol. 1991 Oct; 157(4):721-5.
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Dugast IJ, Papadopoulos P, Zappone E, Jones C, Theriault K, Handelman GJ, Benarous R, Drysdale JW. Identification of two human ferritin H genes on the short arm of chromosome 6. Genomics. 1990 Feb; 6(2):204-11.