Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Moderate hereditary factor VIII deficiency disease
4 0 3 0.25 0 0
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2
6 39 3 0.21 1 1.8E-02
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia
7 0 3 0.20 0 0
Von Willebrand disease, platelet type
8 0 3 0.19 0 0
CUI: C1282971
Disease: von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2B
8 12 3 0.19 1 3.6E-02
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency
9 0 3 0.18 0 0
CUI: C0019021
Disease: Hemoglobin C Disease
Hemoglobin C Disease
3 0 2 0.17 0 0
CUI: C0472801
Disease: Hemophilia A carrier
Hemophilia A carrier
3 0 2 0.17 0 0
Clinically significant macular edema
3 0 2 0.17 0 0
CUI: C1282974
Disease: von Willebrand disease type 2M
von Willebrand disease type 2M
3 0 2 0.17 0 0
CUI: C1282975
Disease: von Willebrand Disease, Type 2N
von Willebrand Disease, Type 2N
10 11 3 0.17 1 3.7E-02
CUI: C2873786
Disease: Deficiency of factor VII [stable]
Deficiency of factor VII [stable]
3 0 2 0.17 0 0
Mild hereditary factor VIII deficiency disease
11 0 3 0.16 0 0
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired
11 0 3 0.16 0 0
CUI: C1282968
Disease: von Willebrand Disease, Type 2A
von Willebrand Disease, Type 2A
4 0 2 0.15 0 0
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder
4 0 2 0.15 0 0
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity
4 0 2 0.15 0 0
CUI: C0017145
Disease: Gastric Varix
Gastric Varix
5 0 2 0.14 0 0
CUI: C0151445
Disease: Primary Raynaud Phenomenon
Primary Raynaud Phenomenon
5 0 2 0.14 0 0
Thrombocytopenia due to sequestration
5 0 2 0.14 0 0
Coagulation factor deficiency syndrome
13 0 3 0.14 0 0
CUI: C0399406
Disease: Irreversible pulpitis
Irreversible pulpitis
5 0 2 0.14 0 0
CUI: C0267370
Disease: Angiodysplasia of colon
Angiodysplasia of colon
6 0 2 0.13 0 0
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency
6 0 2 0.13 0 0
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency
7 0 2 0.12 0 0