 Hemoglobin C Disease
"Hemoglobin C Disease" 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 disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
| Descriptor ID |
D006445
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| MeSH Number(s) |
C15.378.071.141.150.490 C15.378.420.463 C16.320.070.490 C16.320.365.463
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| Concept/Terms |
Hemoglobin C Disease- Hemoglobin C Disease
- C Disease, Hemoglobin
- C Diseases, Hemoglobin
- Hemoglobin C Diseases
- Hemoglobin-C Disease
- Hemoglobin-C Diseases
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Below are MeSH descriptors whose meaning is more general than "Hemoglobin C Disease".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin C Disease".
This graph shows the total number of publications written about "Hemoglobin C Disease" by people in this website by year, and whether "Hemoglobin C Disease" 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 |
|---|
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemoglobin C Disease" by people in Profiles.
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Jacobs JW, Sharma D, Stephens LD, Figueroa Villalba CA, Rinder HM, Woo JS, Wheeler AP, Gerberi D, Goel R, Tormey CA, Booth GS, Bloch EM, Adkins BD. Thrombosis risk with haemoglobin C trait and haemoglobin C disease: A systematic review. Br J Haematol. 2024 Apr; 204(4):1500-1506.
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Field JJ, Strunk RC, Knight-Perry JE, Blinder MA, Townsend RR, DeBaun MR. Urinary cysteinyl leukotriene E4 significantly increases during pain in children and adults with sickle cell disease. Am J Hematol. 2009 Apr; 84(4):231-3.
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