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ENTRY	nt06514
Name	Coagulation cascade
Category	Pathway view; Immune system
Pathway	hsa04610
Disease	H00219 Hemophilia H00223 Inherited thrombophilia H01006 Hereditary angioedema
Display	drug-target relation   disease type

N01506        FXII deficiency/HAE3 N01507        FXI deficiency N01508        HEMB/THPH8 N01509        HEMA     VWD   N01503        FVII deficiency/MI   N01510        FX deficiency N01511        FV deficiency/THPH2/BDCHS N01512        FII deficiency/THPH1 N01513        Afibrinogenemia/Amyloidosis     Afibrinogenemia     Afibrinogenemia N01514        FXIIIA deficiency/MI     FXIIIB deficiency N01521        THPH10   N01518        PLG deficiency/HAE4 N01524        PAI-1 deficiency N01522        a2-PI deficiency N01523        A1AT deficiency/COPD   N01515        THPH3/4     THPH12     THPH5/6   N01516        PKKD N01517        HAE6   N01520        C1NH deficiency/HAE1/2 N01519        AT deficiency/THPH7

FXII deficiency	H00941	Factor XII deficiency
HAE3	H01006	Hereditary angioedema
FXI deficiency	H00938	Factor XI deficiency
HEMB	H00219	Hemophilia
THPH8	H00223	Inherited thrombophilia
HEMA	H00219	Hemophilia
VWD	H02092	von Willebrand disease
	H00219	Hemophilia
FVII deficiency	H02256	Factor VII deficiency
MI	H01730	Myocardial infarction
FX deficiency	H02257	Factor X deficiency
FV deficiency	H00220	Factor V deficiency
THPH2	H00223	Inherited thrombophilia
BDCHS	H01433	Budd-Chiari syndrome
FII deficiency	H01254	Congenital prothrombin deficiency
THPH1	H00223	Inherited thrombophilia
Afibrinogenemia	H00222	Afibrinogenemia
Amyloidosis	H00845	Familial amyloidosis
FXIIIA deficiency	H00945	Factor XIII deficiency
FXIIIB deficiency	H00945	Factor XIII deficiency
THPH10	H00223	Inherited thrombophilia
PLG deficiency	H01206	Plasminogen deficiency
HAE4	H01006	Hereditary angioedema
PAI-1 deficiency	H01106	Plasminogen activator inhibitor type 1 deficiency
a2-PI deficiency	H00983	Alpha-2-plasmin inhibitor (a2-PI) deficiency
A1AT deficiency	H01103	Alpha-1-antitrypsin deficiency
COPD	H01714	Chronic obstructive pulmonary disease (COPD)
THPH3	H00223	Inherited thrombophilia
THPH12	H00223	Inherited thrombophilia
THPH5	H00223	Inherited thrombophilia
PKKD	H01078	Fletcher factor deficiency
HAE6	H01006	Hereditary angioedema
C1NH deficiency	H00106	Complement regulatory protein defects
HAE1	H01006	Hereditary angioedema
AT deficiency	H01381	Antithrombin III deficiency
THPH7	H00223	Inherited thrombophilia