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Hypoprothrombinemias [hypoprotrombinemie]

topical
4
Terms

deficience protrombinu
deficit faktoru II
deficit protrombinu
hypoprotrombinémie
nedostatek faktoru II
nedostatek prothrombinu
nedostatek protrombinu

 

Deficiency, Factor II
Factor II Deficiency
Hypoprothrombinemia
Prothrombin Deficiency

Persistent link   https://www.medvik.cz/link/D007020
Definition

Absence or reduced levels of PROTHROMBIN in the blood.

DUI
D007020 MeSH Browser
CUI
M0010925

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
CN
congenital
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 2
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 978
C15.378.100 Blood Coagulation Disorders 603
C15.378.100.100 Blood Coagulation Disorders, Inherited 64
C15.378.100.100.037 Activated Protein C Resistance 106
C15.378.100.100.056 Afibrinogenemia 40
C15.378.100.100.075 Antithrombin III Deficiency 24
C15.378.100.100.080 Bernard-Soulier Syndrome 9
C15.378.100.100.300 Factor V Deficiency 7
C15.378.100.100.310 Factor VII Deficiency 6
C15.378.100.100.320 Factor X Deficiency 2
C15.378.100.100.325 Factor XI Deficiency 12
C15.378.100.100.330 Factor XII Deficiency 8
C15.378.100.100.335 Factor XIII Deficiency 4
C15.378.100.100.500 Hemophilia A 704
C15.378.100.100.510 Hemophilia B 221
C15.378.100.100.515 Hermanski-Pudlak Syndrome 7
C15.378.100.100.550 Hypoprothrombinemias 4
C15.378.100.100.690 Protein C Deficiency 32
C15.378.100.100.820 Thrombasthenia 7
C15.378.100.100.900 von Willebrand Diseases 106
C15.378.100.100.970 Wiskott-Aldrich Syndrome 20
C15.378.100.141 Coagulation Protein Disorders 53
C15.378.100.141.036 Activated Protein C Resistance 106
C15.378.100.141.072 Afibrinogenemia 40
C15.378.100.141.300 Factor V Deficiency 7
C15.378.100.141.310 Factor VII Deficiency 6
C15.378.100.141.320 Factor X Deficiency 2
C15.378.100.141.325 Factor XI Deficiency 12
C15.378.100.141.330 Factor XII Deficiency 8
C15.378.100.141.335 Factor XIII Deficiency 4
C15.378.100.141.500 Hemophilia A 704
C15.378.100.141.510 Hemophilia B 221
C15.378.100.141.550 Hypoprothrombinemias 4
C15.378.100.141.900 von Willebrand Diseases 106
C15.378.463 Hemorrhagic Disorders 96
C15.378.463.067 Afibrinogenemia 40
C15.378.463.080 Bernard-Soulier Syndrome 9
C15.378.463.250 Disseminated Intravascular Coagulation 212
C15.378.463.300 Factor V Deficiency 7
C15.378.463.310 Factor VII Deficiency 6
C15.378.463.320 Factor X Deficiency 2
C15.378.463.325 Factor XI Deficiency 12
C15.378.463.330 Factor XII Deficiency 8
C15.378.463.335 Factor XIII Deficiency 4
C15.378.463.500 Hemophilia A 704
C15.378.463.510 Hemophilia B 221
C15.378.463.515 Hemostatic Disorders 50
C15.378.463.550 Hypoprothrombinemias 4
C15.378.463.735 Platelet Storage Pool Deficiency 1
C15.378.463.740 Purpura, Thrombocytopenic, Idiopathic 171
C15.378.463.810 Thrombasthenia 7
C15.378.463.825 Thrombocythemia, Essential 95
C15.378.463.841 Vitamin K Deficiency 42
C15.378.463.920 von Willebrand Diseases 106
C15.378.463.950 Waterhouse-Friderichsen Syndrome 11
C15.378.463.960 Wiskott-Aldrich Syndrome 20
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 221
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.099.037 Activated Protein C Resistance 106
C16.320.099.056 Afibrinogenemia 40
C16.320.099.075 Antithrombin III Deficiency 24
C16.320.099.080 Bernard-Soulier Syndrome 9
C16.320.099.300 Factor V Deficiency 7
C16.320.099.310 Factor VII Deficiency 6
C16.320.099.320 Factor X Deficiency 2
C16.320.099.325 Factor XI Deficiency 12
C16.320.099.330 Factor XII Deficiency 8
C16.320.099.335 Factor XIII Deficiency 4
C16.320.099.417 Gray Platelet Syndrome 1
C16.320.099.500 Hemophilia A 704
C16.320.099.510 Hemophilia B 221
C16.320.099.515 Hermanski-Pudlak Syndrome 7
C16.320.099.550 Hypoprothrombinemias 4
C16.320.099.690 Protein C Deficiency 32
C16.320.099.820 Thrombasthenia 7
C16.320.099.920 von Willebrand Diseases 106
C16.320.099.970 Wiskott-Aldrich Syndrome 20

Acquired hypoprothrombinemia Disease MeSH Browser

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