Antithrombin III Deficiency [nedostatek antitrombinu III]

topical
24
Terms

antithrombin III - nedostatek
dědičný deficit antitrombinu III
dědičný nedostatek antitrombinu
deficience antitrombinu III
deficit antitrombinu III
nedostatek antithrombinu III
vrozený deficit antitrombinu III

 

Antithrombin 3 Deficiency
Congenital Antithrombin III Deficiency
Deficiency, Antithrombin III
Hereditary Antithrombin Deficiency

Persistent link   https://www.medvik.cz/link/D020152
Definition

An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis.

DUI
D020152 MeSH Browser
CUI
M0029883
Previous indexing
Antithrombin III/deficiency (1979-1998); Antithrombins/deficiency (1971-1978)
History note
1999
Public note
1999

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 2
CN
congenital 1
DI
diagnosis 4
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 3
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 1
EH
ethnology 0
ET
etiology 0
GE
genetics 6
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 1
PP
physiopathology 0
PC
prevention & control 1
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 0
TH
therapy 1
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 973
C15.378.100 Blood Coagulation Disorders 599
C15.378.100.100 Blood Coagulation Disorders, Inherited 61
C15.378.100.100.037 Activated Protein C Resistance 105
C15.378.100.100.056 Afibrinogenemia 39
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 688
C15.378.100.100.510 Hemophilia B 214
C15.378.100.100.515 Hermanski-Pudlak Syndrome 7
C15.378.100.100.550 Hypoprothrombinemias 4
C15.378.100.100.690 Protein C Deficiency 31
C15.378.100.100.820 Thrombasthenia 7
C15.378.100.100.900 von Willebrand Diseases 103
C15.378.100.100.970 Wiskott-Aldrich Syndrome 20
C15.378.147 Blood Protein Disorders 126
C15.378.147.142 Agammaglobulinemia 113
C15.378.147.150 Antithrombin III Deficiency 24
C15.378.147.333 Dysgammaglobulinemia 10
C15.378.147.542 Hypergammaglobulinemia 55
C15.378.147.607 Hypoproteinemia 27
C15.378.147.780 Paraproteinemias 285
C15.378.147.880 Protein C Deficiency 31
C15.378.147.890 Protein S Deficiency 18
C15.378.925 Thrombophilia 424
C15.378.925.050 Activated Protein C Resistance 105
C15.378.925.075 Antithrombin III Deficiency 24
C15.378.925.220 Disseminated Intravascular Coagulation 209
C15.378.925.795 Protein C Deficiency 31
C15.378.925.800 Protein S Deficiency 18
C15.378.925.850 Purpura, Thrombotic Thrombocytopenic 94
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.099 Blood Coagulation Disorders, Inherited 61
C16.320.099.037 Activated Protein C Resistance 105
C16.320.099.056 Afibrinogenemia 39
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 688
C16.320.099.510 Hemophilia B 214
C16.320.099.515 Hermanski-Pudlak Syndrome 7
C16.320.099.550 Hypoprothrombinemias 4
C16.320.099.690 Protein C Deficiency 31
C16.320.099.820 Thrombasthenia 7
C16.320.099.920 von Willebrand Diseases 103
C16.320.099.970 Wiskott-Aldrich Syndrome 20

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