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
|
| 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.
Below are the most recent publications written about "Blood Coagulation Disorders, Inherited" by people in Profiles.
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Review of Inherited Coagulation Disorders. Anesth Prog. 2024 Jul 08; 71(2):87-95.
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A de novo germline RUNX1 variant preceding development of concurrent T-lymphoblastic leukemia and myelodysplastic syndrome. Leuk Lymphoma. 2024 Sep; 65(9):1357-1361.
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Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradation. Blood Adv. 2021 02 09; 5(3):687-699.
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Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Circulation. 2019 01 29; 139(5):620-635.
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Test-retest properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire and its constituent domains. Haemophilia. 2019 Jan; 25(1):75-83.
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Rare coagulation disorders: fibrinogen, factor VII and factor XIII. Haemophilia. 2016 Jul; 22 Suppl 5:61-5.
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Menstrual bleeding patterns and prevalence of bleeding disorders in a multidisciplinary adolescent haematology clinic. Haemophilia. 2013 Jan; 19(1):71-5.
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Opinions on radiosynovectomy for chronic haemophilic synovitis: point/counterpoint. Haemophilia. 2012 Nov; 18(6):836-42.
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Surveillance of female patients with inherited bleeding disorders in United States Haemophilia Treatment Centres. Haemophilia. 2011 Jul; 17 Suppl 1:6-13.
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High prevalence of dysfibrinogenemia among patients with chronic thromboembolic pulmonary hypertension. Blood. 2009 Aug 27; 114(9):1929-36.