"Hemoglobin SC 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.
One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.
| Descriptor ID |
D006450
|
| MeSH Number(s) |
C15.378.071.141.150.150.440 C15.378.420.155.440 C16.320.070.150.440 C16.320.365.155.440
|
| Concept/Terms |
Hemoglobin SC Disease- Hemoglobin SC Disease
- Disease, Hemoglobin SC
- Diseases, Hemoglobin SC
- Hemoglobin SC Diseases
- SC Disease, Hemoglobin
- SC Diseases, Hemoglobin
- Sickle Cell Hemoglobin C Disease
- SC Disease
- Disease, SC
- Diseases, SC
- SC Diseases
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobin SC Disease".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Anemia, Sickle Cell [C15.378.071.141.150.150]
- Hemoglobin SC Disease [C15.378.071.141.150.150.440]
- Hemoglobinopathies [C15.378.420]
- Anemia, Sickle Cell [C15.378.420.155]
- Hemoglobin SC Disease [C15.378.420.155.440]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Anemia, Sickle Cell [C16.320.070.150]
- Hemoglobin SC Disease [C16.320.070.150.440]
- Hemoglobinopathies [C16.320.365]
- Anemia, Sickle Cell [C16.320.365.155]
- Hemoglobin SC Disease [C16.320.365.155.440]
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin SC Disease".
This graph shows the total number of publications written about "Hemoglobin SC Disease" by people in this website by year, and whether "Hemoglobin SC 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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Hemoglobin SC Disease" by people in Profiles.
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Characterising the prevalence of overweight and obese status among adults with sickle cell disease. Br J Haematol. 2023 03; 200(5):633-642.
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The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial. Br J Haematol. 2011 Mar; 152(6):771-6.
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Stroke prevention in sickle cell disease. Curr Opin Hematol. 2000 Mar; 7(2):101-5.
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Laboratory recognition of a rare hemoglobinopathy: hemoglobins SS and SG(Philadelphia) associated with alpha-thalassemia-2. Arch Pathol Lab Med. 1999 Oct; 123(10):963-6.
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Hip arthroplasty in patients with sickle-cell haemoglobinopathy. J Bone Joint Surg Br. 1992 May; 74(3):367-71.
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Stroke in sickle cell disease. J Med Assoc Ga. 1986 May; 75(5):271-4.