 Factor VII Deficiency
"Factor VII Deficiency" 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.
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.
| Descriptor ID |
D005168
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| MeSH Number(s) |
C15.378.100.100.310 C15.378.100.141.310 C15.378.463.310 C16.320.099.310
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| Concept/Terms |
Factor VII Deficiency- Factor VII Deficiency
- Deficiency, Factor Seven
- Deficiencies, Factor Seven
- Factor Seven Deficiencies
- Factor Seven Deficiency
- Hypoproconvertinemia
- Hypoproconvertinemias
- Deficiency, Factor VII
- Deficiencies, Factor VII
- Factor VII Deficiencies
- Deficiency, Factor 7
- Deficiencies, Factor 7
- Factor 7 Deficiencies
- Factor 7 Deficiency
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Below are MeSH descriptors whose meaning is more general than "Factor VII Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Factor VII Deficiency".
This graph shows the total number of publications written about "Factor VII Deficiency" by people in this website by year, and whether "Factor VII Deficiency" 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 |
|---|
| 2005 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Factor VII Deficiency" by people in Profiles.
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Barbour JR, Iorio ML, Gangopadhyay N, Myckatyn TM. Lower extremity salvage complicated by recurrent microvascular thrombosis in a patient with congenital factor VII deficiency. Am Surg. 2014 Apr; 80(4):417-9.
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MacLaren R, Weber LA, Brake H, Gardner MA, Tanzi M. A multicenter assessment of recombinant factor VIIa off-label usage: clinical experiences and associated outcomes. Transfusion. 2005 Sep; 45(9):1434-42.
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Chaing S, Clarke B, Sridhara S, Chu K, Friedman P, VanDusen W, Roberts HR, Blajchman M, Monroe DM, High KA. Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor. Blood. 1994 Jun 15; 83(12):3524-35.
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Johnson CA, Chung KS, McGrath KM, Bean PE, Roberts HR. Characterization of a variant prothrombin in a patient congenitally deficient in factors II, VII, IX and X. Br J Haematol. 1980 Mar; 44(3):461-9.
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