Protein C Deficiency [nedostatek proteinu C]

topical
31
Terms

deficit proteinu C
protein C - nedostatek

 

Deficiency, Protein C
Hereditary Thrombophilia Due To Protein C Deficiency

Persistent link   https://www.medvik.cz/link/D020151
Definition

An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.)

DUI
D020151 MeSH Browser
CUI
M0029882
Previous indexing
Blood Proteins (1981-1987); Glycoproteins (1981-1987); Protein C (1987-1998)
History note
1999
Public note
1999

C Diseases
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
C15.378.147.142 Agammaglobulinemia 114
C15.378.147.333 Dysgammaglobulinemia 10
C15.378.147.542 Hypergammaglobulinemia 55
C15.378.147.607 Hypoproteinemia 27
C15.378.147.780 Paraproteinemias 290
C15.378.147.880 Protein C Deficiency 31
C15.378.147.890 Protein S Deficiency 18
C15.378.925 Thrombophilia 426
C15.378.925.795 Protein C Deficiency 31
C15.378.925.800 Protein S Deficiency 18
C16.320.099.056 Afibrinogenemia 39
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

Congenital thrombotic disease, due to Protein C deficiency Disease MeSH Browser

Protein C Deficiency, Acquired Disease MeSH Browser

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant Disease MeSH Browser

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive Disease MeSH Browser