"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
|
| MeSH Number(s) |
C15.378.100.100.320 C15.378.100.141.320 C15.378.463.320 C16.320.099.320
|
| 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
|
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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 2 | 1 | 3 |
| 2020 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Factor X Deficiency" by people in Profiles.
-
Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection. Int J Lab Hematol. 2020 12; 42(6):e277-e279.
-
Empirically Reduced Dosages of Tinzaparin in Patients with Moderate-to-Severe Renal Insufficiency Lead to Inadequate Anti-Xa Levels. Nephron. 2017; 137(2):113-123.
-
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway. Blood. 2017 08 03; 130(5):666-676.
-
Complex formation with pentraxin-2 regulates factor X plasma levels and macrophage interactions. Blood. 2017 04 27; 129(17):2443-2454.
-
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency. Eur J Clin Invest. 2015 Oct; 45(10):1087-91.
-
Femur fracture in a woman with severe factor X deficiency - an experience using factor X concentrate in surgery. Haemophilia. 2013 Nov; 19(6):e369-70.
-
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency. Br J Haematol. 2002 Jun; 117(3):685-92.