"Hypoprothrombinemias" 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.
Absence or reduced levels of PROTHROMBIN in the blood.
| Descriptor ID |
D007020
|
| MeSH Number(s) |
C15.378.100.100.550 C15.378.100.141.550 C15.378.463.550 C16.320.099.550
|
| Concept/Terms |
Hypoprothrombinemias- Hypoprothrombinemias
- Prothrombin Deficiency
- Deficiencies, Prothrombin
- Deficiency, Prothrombin
- Prothrombin Deficiencies
- Hypoprothrombinemia
- Deficiency, Factor II
- Deficiencies, Factor II
- Factor II Deficiencies
- Factor II Deficiency
|
Below are MeSH descriptors whose meaning is more general than "Hypoprothrombinemias".
Below are MeSH descriptors whose meaning is more specific than "Hypoprothrombinemias".
This graph shows the total number of publications written about "Hypoprothrombinemias" by people in this website by year, and whether "Hypoprothrombinemias" 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 |
|---|
| 1997 | 2 | 0 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hypoprothrombinemias" by people in Profiles.
-
Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, Rappaport EF. Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP). Blood Coagul Fibrinolysis. 1997 Sep; 8(6):337-43.
-
Poort SR, Landolfi R, Bertina RM. Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency. Thromb Haemost. 1997 Apr; 77(4):610-5.