 Factor X Deficiency
"Factor X 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.
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
| Descriptor ID |
D005171
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| MeSH Number(s) |
C15.378.100.100.320 C15.378.100.141.320 C15.378.463.320 C16.320.099.320
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| Concept/Terms |
Factor X Deficiency- Factor X Deficiency
- Deficiency, Factor Ten
- Deficiencies, Factor Ten
- Factor Ten Deficiencies
- Ten Deficiencies, Factor
- Factor 10 Deficiency
- Factor Ten Deficiency
- Stuart-Prower Factor Deficiency
- Stuart Prower Factor Deficiency
- Deficiency, Stuart-Prower
- Deficiency, Stuart Prower
- Stuart-Prower Deficiency
- Stuart Prower Deficiency
- Deficiency, Stuart-Prower Factor
- Deficiency, Stuart Prower Factor
- Deficiency, Factor 10
- Deficiencies, Factor 10
- Factor 10 Deficiencies
- Deficiency, Factor X
- Deficiencies, Factor X
- Factor X Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Factor X Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Factor X Deficiency".
This graph shows the total number of publications written about "Factor X Deficiency" by people in this website by year, and whether "Factor X Deficiency" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
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Below are the most recent publications written about "Factor X Deficiency" by people in Profiles.
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Lee G, Duan-Porter W, Metjian AD. Acquired, non-amyloid related factor X deficiency: review of the literature. Haemophilia. 2012 Sep; 18(5):655-63.
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La Rosa FG, Clarke SH, Lefkowitz JB. Brodifacoum intoxication with marijuana smoking. Arch Pathol Lab Med. 1997 Jan; 121(1):67-9.
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Watzke HH, Lechner K, Roberts HR, Reddy SV, Welsch DJ, Friedman P, Mahr G, Jagadeeswaran P, Monroe DM, High KA. Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg"). J Biol Chem. 1990 Jul 15; 265(20):11982-9.
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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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