 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 |
|---|
| 2009 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hemoglobin C Disease" by people in Profiles.
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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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