 von Willebrand Diseases
"von Willebrand Diseases" 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.
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
| Descriptor ID |
D014842
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| MeSH Number(s) |
C15.378.100.100.900 C15.378.100.141.900 C15.378.140.900 C15.378.463.920 C16.320.099.920
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| Concept/Terms |
von Willebrand Diseases- von Willebrand Diseases
- Hemophilia, Vascular
- Vascular Hemophilia
- Vascular Hemophilias
- Vascular Pseudohemophilia
- Pseudohemophilia, Vascular
- Pseudohemophilias, Vascular
- Vascular Pseudohemophilias
- Von Willebrand's Factor Deficiency
- Von Willebrand Disorder
- Disorder, Von Willebrand
- von Willebrand's Disease
- von Willebrand's Diseases
- Angiohemophilia
- Angiohemophilias
- von Willebrand Disease
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Below are MeSH descriptors whose meaning is more general than "von Willebrand Diseases".
Below are MeSH descriptors whose meaning is more specific than "von Willebrand Diseases".
This graph shows the total number of publications written about "von Willebrand Diseases" by people in this website by year, and whether "von Willebrand Diseases" 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 | | 2001 | 0 | 1 | 1 | | 2004 | 1 | 0 | 1 | | 2006 | 0 | 1 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 2 | 0 | 2 | | 2018 | 1 | 1 | 2 | | 2020 | 1 | 0 | 1 | | 2022 | 2 | 0 | 2 | | 2023 | 2 | 0 | 2 | | 2024 | 1 | 0 | 1 | | 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "von Willebrand Diseases" by people in Profiles.
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Jiang D, Wang M, Wheeler AP, Croteau SE. 2025 Clinical Trials Update on Hemophilia, VWD, and Rare Inherited Bleeding Disorders. Am J Hematol. 2025 Apr; 100(4):666-684.
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Simoneau J, Tay C, Wheeler A, Amos L, McCormick M, Collado Y, Brown M, Weyand AC. Association between hemoglobin values and VWF assays: a multicenter investigation. Blood Adv. 2024 03 12; 8(5):1152-1154.
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Ragni MV, Rothenberger SD, Feldman R, Nance D, Leavitt AD, Malec L, Kulkarni R, Sidonio R, Kraut E, Lasky J, Pruthi R, Angelini D, Philipp C, Hwang N, Wheeler AP, Seaman C, Machin N, Xavier F, Meyer M, Bellissimo D, Humphreys G, Smith KJ, Merricks EP, Nichols TC, Ivanco D, Vehec D, Koerbel G, Althouse AD. Recombinant von Willebrand factor and tranexamic acid for heavy menstrual bleeding in patients with mild and moderate von Willebrand disease in the USA (VWDMin): a phase 3, open-label, randomised, crossover trial. Lancet Haematol. 2023 Aug; 10(8):e612-e623.
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Sidonio RF, Bryant PC, Di Paola J, Hale S, Heiman M, Horowitz GS, Humphrey C, Jaffray J, Joyner LC, Kasthuri R, Konkle BA, Kouides PA, Montgomery R, Neeves K, Randi AM, Scappe N, Tarango C, Tickle K, Trapane P, Wang M, Waters B, Flood VH. Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for mucocutaneous bleeding disorders. Expert Rev Hematol. 2023 03; 16(sup1):39-54.
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Ng CJ, Liu A, Venkataraman S, Ashworth KJ, Baker CD, O'Rourke R, Vibhakar R, Jones KL, Di Paola J. Single-cell transcriptional analysis of human endothelial colony-forming cells from patients with low VWF levels. Blood. 2022 04 07; 139(14):2240-2251.
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Sadler B, Minard CG, Haller G, Gurnett CA, O'Brien SH, Wheeler A, Jain S, Sharma M, Zia A, Kulkarni R, Mullins E, Ragni MV, Sidonio R, Dietrich JE, Kouides PA, Di Paola J, Srivaths L. Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations. Blood Adv. 2022 01 25; 6(2):420-428.
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Jaffray J, Staber JM, Malvar J, Sidonio R, Haley KM, Stillings A, Weyand A, Hege K, Jain S, Gupta S, Agnew C, Wheeler A, Pawar A, Sharma M, Chitlur M, O'Brien SH, Kouides P. Laboratory misdiagnosis of von Willebrand disease in post-menarchal females: A multi-center study. Am J Hematol. 2020 09; 95(9):1022-1029.
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Rao ES, Ng CJ. Current approaches to diagnostic testing in von Willebrand Disease. Transfus Apher Sci. 2018 Aug; 57(4):463-465.
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Ng CJ, Di Paola J. von Willebrand Disease: Diagnostic Strategies and Treatment Options. Pediatr Clin North Am. 2018 06; 65(3):527-541.
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Gupta S, Heiman M, Duncan N, Hinckley J, Di Paola J, Shapiro AD. Variable bleeding phenotype in an Amish pedigree with von Willebrand disease. Am J Hematol. 2016 Oct; 91(10):E431-5.
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