Blood Coagulation Disorders, Inherited [dědičné koagulopatie]

topical
64
Terms

dědičné poruchy koagulace
koagulopatie dědičné
vrozené koagulopatie

 

Coagulation Disorders, Inherited
Hereditary Blood Coagulation Disorders
Hereditary Coagulation Disorders
Inherited Blood Coagulation Disorders
Inherited Coagulation Disorders

Persistent link   https://www.medvik.cz/link/D025861
Definition

Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.

DUI
D025861 MeSH Browser
CUI
M0376236
Previous indexing
Blood Coagulation Disorders (1995-2001)
History note
2002
Public note
2002

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 3
CO
complications 9
DI
diagnosis 25
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 9
EC
economics 1
EM
embryology
EN
enzymology
EP
epidemiology 5
EH
ethnology
ET
etiology 4
GE
genetics 13
HI
history 3
IM
immunology 1
ME
metabolism
MI
microbiology
MO
mortality 1
NU
nursing
PS
parasitology
PA
pathology 4
PP
physiopathology 6
PC
prevention & control 2
PX
psychology
RT
radiotherapy
RH
rehabilitation 1
SU
surgery
TH
therapy 24
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
C15.378.100.100.970 Wiskott-Aldrich Syndrome 20
C15.378.100.141 Coagulation Protein Disorders 53
C15.378.100.220 Disseminated Intravascular Coagulation 210
C15.378.100.452 Ecchymosis 10
C15.378.100.685 Platelet Storage Pool Deficiency 1
C15.378.100.800 Protein S Deficiency 18
C15.378.100.802 Purpura 109
C15.378.100.832 Thrombocythemia, Essential 94
C15.378.100.876 Thromboinflammation 3
C15.378.100.920 Vitamin K Deficiency 42
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
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
C16.320.099.970 Wiskott-Aldrich Syndrome 20
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Athrombia, Essential Disease MeSH Browser

Bleeding Disorder Due To P2RY12 Defect Disease MeSH Browser

Dysprothrombinemia Disease MeSH Browser

Factors VIII, IX And XI, Combined Deficiency of Disease MeSH Browser

Familial Multiple Coagulation Factor Deficiency II Disease MeSH Browser

Familial Multiple Coagulation Factor Deficiency IV Disease MeSH Browser

Familial Multiple Coagulation Factor Deficiency VI Disease MeSH Browser

Passovoy Factor Disease MeSH Browser

Pechet Factor Deficiency Disease MeSH Browser

Platelet Disorder, Familial, with Associated Myeloid Malignancy Disease MeSH Browser

Prolonged Bleeding Time, Brachydactyly, and Mental Retardation Disease MeSH Browser

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 Disease MeSH Browser

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 2 Disease MeSH Browser

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