"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 |
---|
2004 | 1 | 0 | 1 |
2017 | 0 | 1 | 1 |
2022 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hemoglobin SC Disease" by people in Profiles.
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Early ML, Luo A, Solow M, Matusiak K, Eke AC, Shehata N, August P, Kuo KHM, Lanzkron S, Malinowski AK, Pecker LH. Natural history of blood pressure in sickle cell disease pregnancy. Br J Haematol. 2024 02; 204(2):658-667.
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Kim A, Assarzadegan N, Anders RA, Oshima K, Chaturvedi S, Weeks S, Kohli R, Lanzkron S, Gurakar A, Garonzik-Wang J, Chen PH. Liver Transplant in Hemoglobin SC Disease and Autoimmune Hepatitis: A Case Report. Exp Clin Transplant. 2022 04; 20(4):429-432.
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Misra I, Glasgow J, Moosavy F. Fat Emboli Syndrome. Del Med J. 2017 May; 89(5):148-150.
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Wagner SC, Eschelman DJ, Gonsalves CF, Bonn J, Sullivan KL. Infectious complications of implantable venous access devices in patients with sickle cell disease. J Vasc Interv Radiol. 2004 Apr; 15(4):375-8.
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Talacki CA, Rappaport E, Schwartz E, Surrey S, Ballas SK. Beta-globin gene cluster haplotypes in Hb C heterozygotes. Hemoglobin. 1990; 14(3):229-40.
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Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. The xerocytosis of Hb SC disease. Blood. 1987 Jan; 69(1):124-30.