Blood Coagulation Disorders, Inherited
"Blood Coagulation Disorders, Inherited" 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.
Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
Descriptor ID |
D025861
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MeSH Number(s) |
C15.378.100.100 C16.320.099
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Concept/Terms |
Blood Coagulation Disorders, Inherited- Blood Coagulation Disorders, Inherited
- Inherited Blood Coagulation Disorders
- Hereditary Coagulation Disorders
- Coagulation Disorder, Hereditary
- Coagulation Disorders, Hereditary
- Hereditary Coagulation Disorder
- Coagulation Disorders, Inherited
- Inherited Coagulation Disorders
- Coagulation Disorder, Inherited
- Inherited Coagulation Disorder
- Hereditary Blood Coagulation Disorders
|
Below are MeSH descriptors whose meaning is more general than "Blood Coagulation Disorders, Inherited".
Below are MeSH descriptors whose meaning is more specific than "Blood Coagulation Disorders, Inherited".
This graph shows the total number of publications written about "Blood Coagulation Disorders, Inherited" by people in this website by year, and whether "Blood Coagulation Disorders, Inherited" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2002 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
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Below are the most recent publications written about "Blood Coagulation Disorders, Inherited" by people in Profiles.
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Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patients. Am J Hematol. 2010 May; 85(5):395-6.
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Antithrombin alfa in hereditary antithrombin deficient patients: A phase 3 study of prophylactic intravenous administration in high risk situations. Thromb Haemost. 2008 Mar; 99(3):616-22.
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Systemic-to-pulmonary artery shunt thrombosis in a neonate with factor V Leiden mutation. Ann Thorac Surg. 2002 Dec; 74(6):2179-81.