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: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
14 26 13 0.23 24 5.6E-02
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement
15 42 9 0.15 15 3.3E-02
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery
11 0 5 8.2E-02 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1
39 26 7 8.0E-02 1 2.2E-03
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis
13 0 5 7.9E-02 0 0
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
16 36 5 7.6E-02 9 2.0E-02
CUI: C0523688
Disease: Hemopexin measurement
Hemopexin measurement
4 5 4 7.3E-02 2 4.7E-03
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration
49 69 7 7.2E-02 2 4.0E-03
CUI: C0032797
Disease: Postpartum Hemorrhage
Postpartum Hemorrhage
6 0 4 7.0E-02 0 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma
6 0 4 7.0E-02 0 0
CUI: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency
14 0 4 6.2E-02 0 0
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
15 16 4 6.1E-02 2 4.5E-03
CUI: C0025323
Disease: Menorrhagia
Menorrhagia
34 0 5 6.0E-02 0 0
Activated Partial Thromboplastin Time measurement
17 44 4 5.9E-02 9 1.9E-02
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
42 0 5 5.4E-02 0 0
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy
85 81 7 5.3E-02 2 4.0E-03
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding
5 0 3 5.3E-02 0 0
Fibroblast Growth Factor 23 Measurement
6 0 3 5.2E-02 0 0
Prolonged bleeding after dental extraction
8 0 3 5.0E-02 0 0
CUI: C1844374
Disease: Persistent bleeding after trauma
Persistent bleeding after trauma
9 0 3 4.9E-02 0 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
117 218 8 4.9E-02 32 5.2E-02
CUI: C0015530
Disease: Hereditary Factor XIII Deficiency
Hereditary Factor XIII Deficiency
10 0 3 4.8E-02 0 0
CUI: C3150275
Disease: COMPLEMENT COMPONENT 2 DEFICIENCY
COMPLEMENT COMPONENT 2 DEFICIENCY
11 0 3 4.8E-02 0 0
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
Atypical Hemolytic Uremic Syndrome
56 42 5 4.7E-02 1 2.1E-03
Exudative age-related macular degeneration
158 109 9 4.4E-02 2 3.7E-03