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
|
MeSH Number(s) |
C15.378.071.141.150.490 C15.378.420.463 C16.320.070.490 C16.320.365.463
|
Concept/Terms |
Hemoglobin C Disease- Hemoglobin C Disease
- C Disease, Hemoglobin
- C Diseases, Hemoglobin
- Hemoglobin C Diseases
- Hemoglobin-C Disease
- Hemoglobin-C Diseases
|
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.
Below are the most recent publications written about "Hemoglobin C Disease" by people in Profiles.
-
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.
|
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|