Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		16 0 8 0.44 0 0
CUI: C0272323
Disease: Moderate hereditary factor VIII deficiency disease
Moderate hereditary factor VIII deficiency disease 		4 0 3 0.27 0 0
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		6 39 3 0.23 4 8.7E-02
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia 		7 0 3 0.21 0 0
CUI: C1280798
Disease: Von Willebrand disease, platelet type
Von Willebrand disease, platelet type 		8 0 3 0.20 0 0
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B 		8 12 3 0.20 1 4.5E-02
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		9 0 3 0.19 0 0
CUI: C0472801
Disease: Hemophilia A carrier
Hemophilia A carrier 		3 0 2 0.18 0 0
CUI: C1282974
Disease: von Willebrand disease type 2M
von Willebrand disease type 2M 		3 0 2 0.18 0 0
CUI: C2873786
Disease: Deficiency of factor VII [stable]
Deficiency of factor VII [stable] 		3 0 2 0.18 0 0
CUI: C3151080
Disease: COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II 		3 0 2 0.18 0 0
CUI: C0272324
Disease: Mild hereditary factor VIII deficiency disease
Mild hereditary factor VIII deficiency disease 		11 0 3 0.17 0 0
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired 		11 0 3 0.17 0 0
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3 		11 17 3 0.17 1 3.7E-02
CUI: C1282968
Disease: von Willebrand Disease, Type 2A
von Willebrand Disease, Type 2A 		4 0 2 0.17 0 0
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		4 0 2 0.17 0 0
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity 		4 0 2 0.17 0 0
CUI: C0017145
Disease: Gastric Varix
Gastric Varix 		5 0 2 0.15 0 0
CUI: C0151445
Disease: Primary Raynaud Phenomenon
Primary Raynaud Phenomenon 		5 0 2 0.15 0 0
CUI: C0272315
Disease: Coagulation factor deficiency syndrome
Coagulation factor deficiency syndrome 		13 0 3 0.15 0 0
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency 		6 0 2 0.14 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 4 0.14 0 0
CUI: C3887523
Disease: Very long chain acyl-CoA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency 		15 0 3 0.14 0 0
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		7 0 2 0.13 0 0
CUI: C1856883
Disease: FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF 		7 0 2 0.13 0 0