KEGG    Network variation - Coagulation cascade
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ENTRYnt06514
NameCoagulation cascade
CategoryPathway view; Immune system
Pathwayhsa04610 Complement and coagulation cascades
DiseaseH00219 Hemophilia
H00223 Inherited thrombophilia
H01006 Hereditary angioedema
Display drug-target relation   disease type
N01506    F12KallikreinF12a
    FXII deficiency/HAE3 F12*
N01507      F11F12aF11a
    FXI deficiency   F11*
N01508        F9F11aF9a(F9a+F8a)
    HEMB/THPH8     F9*
     D1
 |
      
N01509        (F8+VWF)(F10a,F2a)F8a(F9a+F8a)
    HEMA     F8*
    VWD     VWF*
N01503    F7ProteaseF7a(F7a+F3)
    FVII deficiency/MI F7*
N01510    F10((F9a+F8a),(F7a+F3..F10a(F10a+F5a)
    FX deficiency F10*
N01511    F5F2aF5a(F10a+F5a)
    FV deficiency/THPH2/BDCHS F5*
N01512        F2(F10a+F5a)F2a
    FII deficiency/THPH1     F2*
N01513          FGF2aFibrin
    Afibrinogenemia/Amyloidosis       FGA*
    Afibrinogenemia       FGB*
    Afibrinogenemia       FGG*
N01514          F13F2aF13a
    FXIIIA deficiency/MI       F13A1*
    FXIIIB deficiency       F13B*
N01521          SERPIND1F2a
    THPH10       SERPIND1*
N01518    PLG(PLAU,PLAT)Plasmin
    PLG deficiency/HAE4 PLG*
N01524    PAI(PLAU,PLAT)
    PAI-1 deficiency SERPINE1*
N01522      SERPINF2Plasmin
    a2-PI deficiency   SERPINF2*
N01523      SERPINA1(Plasmin,PLAU)
    A1AT deficiency/COPD   SERPINA1*
N01515    PROC(F2a+THBD+PROCR)APC(APC+PROS1)(F5a,F8a)
    THPH3/4 PROC*
    THPH12   THBD*
    THPH5/6       PROS1*
N01516    KLKB1F12aKallikrein
    PKKD KLKB1*
N01517      KNG1KallikreinBradykininBDKRB
    HAE6   KNG1*
N01520    SERPING1(F11a,F12a,Kallikr..
    C1NH deficiency/HAE1/2 SERPING1*
N01519    SERPINC1(F2a,F9a,F10a,F11a..
    AT deficiency/THPH7 SERPINC1*

Disease nameDisease category
FXII deficiency/HAE3H00941Factor XII deficiencyHematologic disease
H01006Hereditary angioedemaCardiovascular disease
FXI deficiencyH00938Factor XI deficiencyHematologic disease
HEMB/THPH8H00219HemophiliaHematologic disease
H00223Inherited thrombophiliaHematologic disease
HEMAH00219HemophiliaHematologic disease
VWDH02092von Willebrand diseaseHematologic disease
H00219HemophiliaHematologic disease
FVII deficiency/MIH02256Factor VII deficiencyHematologic disease
H01730Myocardial infarctionCardiovascular disease
FX deficiencyH02257Factor X deficiencyHematologic disease
FV deficiency/THPH2/BDCHSH00220Factor V deficiencyHematologic disease
H00223Inherited thrombophiliaHematologic disease
H01433Budd-Chiari syndromeDigestive system disease
FII deficiency/THPH1H01254Congenital prothrombin deficiencyHematologic disease
H00223Inherited thrombophiliaHematologic disease
Afibrinogenemia/AmyloidosisH00222AfibrinogenemiaHematologic disease
H00845Familial amyloidosisNervous system disease
AfibrinogenemiaH00222AfibrinogenemiaHematologic disease
FXIIIA deficiency/MIH00945Factor XIII deficiencyHematologic disease
H01730Myocardial infarctionCardiovascular disease
FXIIIB deficiencyH00945Factor XIII deficiencyHematologic disease
THPH10H00223Inherited thrombophiliaHematologic disease
PLG deficiency/HAE4H01206Plasminogen deficiencyHematologic disease
H01006Hereditary angioedemaCardiovascular disease
PAI-1 deficiencyH01106Plasminogen activator inhibitor type 1 deficiencyHematologic disease
a2-PI deficiencyH00983Alpha-2-plasmin inhibitor (a2-PI) deficiencyHematologic disease
A1AT deficiency/COPDH01103Alpha-1-antitrypsin deficiencyInherited metabolic disorder
H01714Chronic obstructive pulmonary disease (COPD)Respiratory system disease
THPH3/4H00223Inherited thrombophiliaHematologic disease
THPH12H00223Inherited thrombophiliaHematologic disease
THPH5/6H00223Inherited thrombophiliaHematologic disease
PKKDH01078Fletcher factor deficiencyHematologic disease
HAE6H01006Hereditary angioedemaCardiovascular disease
C1NH deficiency/HAE1/2H00106Complement regulatory protein defectsPrimary immunodeficiency
H01006Hereditary angioedemaCardiovascular disease
AT deficiency/THPH7H01381Antithrombin III deficiencyHematologic disease
H00223Inherited thrombophiliaHematologic disease


Drug name
D1D02235Desmopressin acetate (USP)