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: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		486 1243 7 1.3E-02 1 8.0E-04
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		1159 704 18 1.5E-02 1 1.4E-03
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 143 3 2.4E-02 2 1.3E-02
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		7 119 4 5.4E-02 3 2.3E-02
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		592 110 21 3.3E-02 2 1.6E-02
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease 		62 78 4 3.1E-02 2 2.2E-02
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		10 73 3 3.8E-02 1 1.2E-02
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		32 68 1 9.8E-03 1 1.2E-02
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		26 63 3 3.2E-02 1 1.3E-02
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		26 63 3 3.2E-02 1 1.3E-02
CUI: C1264040
Disease: von Willebrand Disease, Type 2
von Willebrand Disease, Type 2 		6 39 1 1.3E-02 2 3.9E-02
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3 		11 17 1 1.2E-02 1 3.3E-02
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		60 14 5 4.0E-02 1 3.7E-02
CUI: C1282975
Disease: von Willebrand Disease, Type 2N
von Willebrand Disease, Type 2N 		10 11 1 1.3E-02 1 4.2E-02
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		6 10 3 4.1E-02 2 9.1E-02
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 6 3 3.7E-02 1 5.3E-02
CUI: C4310797
Disease: BLEEDING DISORDER, PLATELET-TYPE, 20
BLEEDING DISORDER, PLATELET-TYPE, 20 		1 4 1 1.4E-02 2 0.12
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time 		39 3 6 5.8E-02 3 0.21
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 3 1.8E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 9 2.5E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 3 2.3E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 15 1.3E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 7 2.2E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 10 4.0E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 4 2.3E-02 0 0