von Willebrand Diseases [von Willebrandova nemoc]

topical
103
Terms

angiohemofilie
vaskulární hemofilie
von Willebrandova choroba
von Willebrandova nemoc - recesivní forma
von Willebrandovy nemoci
Willebrandova nemoc

 

Angiohemophilia
Hemophilia, Vascular
Vascular Pseudohemophilia
von Willebrand Disease
von Willebrand Disease, Recessive Form
Von Willebrand Disorder
von Willebrand's Disease
von Willebrand's Diseases
Von Willebrand's Factor Deficiency

Persistent link   https://www.medvik.cz/link/D014842
Definition

Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.

Annotation
note specific types of Von Willebrand Disease are available
k dispozici jsou i deskriptory specifických typů von Willebrandovy nemoci
DUI
D014842 MeSH Browser
CUI
M0022853
History note
2010(1963)
Public note
2010; see VON WILLEBRAND DISEASE 1999-2009; see VON WILLEBRAND'S DISEASE 1968-1998, see HEMORRHAGIC DIATHESIS 1967, see THROMBOCYTOPATHY 1963-1966

Allowable subheadings

BL
blood 6
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 13
CO
complications 13
DI
diagnosis 47
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 20
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 9
EH
ethnology
ET
etiology 8
GE
genetics 17
HI
history
IM
immunology 1
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 6
PP
physiopathology 6
PC
prevention & control 2
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 29
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 976
C15.378.100 Blood Coagulation Disorders 600
C15.378.100.100 Blood Coagulation Disorders, Inherited 64
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 691
C15.378.100.100.510 Hemophilia B 216
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
C15.378.100.100.900.100 von Willebrand Disease, Type 1 4
C15.378.100.100.900.200 von Willebrand Disease, Type 2 3
C15.378.100.100.900.300 von Willebrand Disease, Type 3 2
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 105
C15.378.100.141.072 Afibrinogenemia 39
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 691
C15.378.100.141.510 Hemophilia B 216
C15.378.100.141.550 Hypoprothrombinemias 4
C15.378.100.141.900 von Willebrand Diseases 103
C15.378.100.141.900.100 von Willebrand Disease, Type 1 4
C15.378.100.141.900.200 von Willebrand Disease, Type 2 3
C15.378.100.141.900.300 von Willebrand Disease, Type 3 2
C15.378.140 Blood Platelet Disorders 123
C15.378.140.120 Bernard-Soulier Syndrome 9
C15.378.140.427 Gray Platelet Syndrome 1
C15.378.140.735 Platelet Storage Pool Deficiency 1
C15.378.140.810 Thrombasthenia 7
C15.378.140.855 Thrombocytopenia 603
C15.378.140.860 Thrombocytosis 61
C15.378.140.900 von Willebrand Diseases 103
C15.378.463 Hemorrhagic Disorders 95
C15.378.463.067 Afibrinogenemia 39
C15.378.463.080 Bernard-Soulier Syndrome 9
C15.378.463.250 Disseminated Intravascular Coagulation 210
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 691
C15.378.463.510 Hemophilia B 216
C15.378.463.515 Hemostatic Disorders 49
C15.378.463.550 Hypoprothrombinemias 4
C15.378.463.735 Platelet Storage Pool Deficiency 1
C15.378.463.740 Purpura, Thrombocytopenic, Idiopathic 172
C15.378.463.810 Thrombasthenia 7
C15.378.463.825 Thrombocythemia, Essential 94
C15.378.463.841 Vitamin K Deficiency 42
C15.378.463.920 von Willebrand Diseases 103
C15.378.463.920.100 von Willebrand Disease, Type 1 4
C15.378.463.920.200 von Willebrand Disease, Type 2 3
C15.378.463.920.300 von Willebrand Disease, Type 3 2
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 1 215
C16.320.099 Blood Coagulation Disorders, Inherited 64
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 691
C16.320.099.510 Hemophilia B 216
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
C16.320.099.920.100 von Willebrand Disease, Type 1 4
C16.320.099.920.200 von Willebrand Disease, Type 2 3
C16.320.099.920.300 von Willebrand Disease, Type 3 2
C16.320.099.970 Wiskott-Aldrich Syndrome 20

Von Willebrand Disease, X-Linked Form Disease MeSH Browser

Von Willebrand disease, platelet type Disease MeSH Browser

Von willebrand factor, deficiency Disease MeSH Browser

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