 Hemochromatosis
"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
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| MeSH Number(s) |
C16.320.565.618.337 C18.452.565.500.480 C18.452.648.618.337
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| 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
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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 |
|---|
| 2000 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2011 | 0 | 1 | 1 | | 2015 | 2 | 0 | 2 | | 2017 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Hemochromatosis" by people in Profiles.
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Gerhard GS, Paynton BV, DiStefano JK. Identification of Genes for Hereditary Hemochromatosis. Methods Mol Biol. 2018; 1706:353-365.
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Raffield LM, Louie T, Sofer T, Jain D, Ipp E, Taylor KD, Papanicolaou GJ, Avil?s-Santa L, Lange LA, Laurie CC, Conomos MP, Thornton TA, Chen YI, Qi Q, Cotler S, Thyagarajan B, Schneiderman N, Rotter JI, Reiner AP, Lin HJ. Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Hum Mol Genet. 2017 05 15; 26(10):1966-1978.
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Colom Steele D, Mojtahed A, Samedi V, Alcorn J. "Ferritin Out" a Cause of Acute Hepatitis. Dig Dis Sci. 2015 Oct; 60(10):2927-9.
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Gelderman MP, Baek JH, Yalamanoglu A, Puglia M, Vallelian F, Burla B, Vostal J, Schaer DJ, Buehler PW. Reversal of hemochromatosis by apotransferrin in non-transfused and transfused Hbbth3/+ (heterozygous B1/B2 globin gene deletion) mice. Haematologica. 2015 May; 100(5):611-22.
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Sundaram SS, Alonso EM, Narkewicz MR, Zhang S, Squires RH. Characterization and outcomes of young infants with acute liver failure. J Pediatr. 2011 Nov; 159(5):813-818.e1.
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Rand EB, Karpen SJ, Kelly S, Mack CL, Malatack JJ, Sokol RJ, Whitington PF. Treatment of neonatal hemochromatosis with exchange transfusion and intravenous immunoglobulin. J Pediatr. 2009 Oct; 155(4):566-71.
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Hiatt T, Trotter JF, Kam I. Hepatocellular carcinoma in a noncirrhotic patient with hereditary hemochromatosis. Am J Med Sci. 2007 Sep; 334(3):228-30.
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Hussain SP, Raja K, Amstad PA, Sawyer M, Trudel LJ, Wogan GN, Hofseth LJ, Shields PG, Billiar TR, Trautwein C, Hohler T, Galle PR, Phillips DH, Markin R, Marrogi AJ, Harris CC. Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases. Proc Natl Acad Sci U S A. 2000 Nov 07; 97(23):12770-5.
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Shneider BL, Setchell KD, Whitington PF, Neilson KA, Suchy FJ. Delta 4-3-oxosteroid 5 beta-reductase deficiency causing neonatal liver failure and hemochromatosis. J Pediatr. 1994 Feb; 124(2):234-8.
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Hambidge KM, Walravens PA. Disorders of mineral metabolism. Clin Gastroenterol. 1982 Jan; 11(1):87-117.
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