Source: CURATED ×
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: C3494186
Disease: Autosomal Hemophilia A
Autosomal Hemophilia A 		2 0 2 1.00 0 0
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		2 0 2 1.00 0 0
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		1 111 1 0.50 27 7.6E-02
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		1 0 1 0.50 0 0
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired 		1 0 1 0.50 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 5 1 0.50 2 7.3E-03
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		4 0 1 0.20 0 0
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		9 0 1 1.0E-01 0 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		21 0 1 4.5E-02 0 0
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		21 0 1 4.5E-02 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		42 0 1 2.3E-02 0 0
CUI: C0087086
Disease: Thrombus
Thrombus 		46 0 1 2.1E-02 0 0
CUI: C0040053
Disease: Thrombosis
Thrombosis 		49 0 1 2.0E-02 0 0
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma 		109 0 1 9.1E-03 0 0
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		477 0 1 2.1E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		0 4 0 0 1 3.7E-03
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation 		0 15 0 0 3 1.1E-02
CUI: C3890932
Disease: FACTOR VIII (OKAYAMA) PHENOTYPE
FACTOR VIII (OKAYAMA) PHENOTYPE 		0 1 0 0 1 3.7E-03
CUI: C4017565
Disease: FACTOR VIII (EAST HARTFORD) PHENOTYPE
FACTOR VIII (EAST HARTFORD) PHENOTYPE 		0 1 0 0 1 3.7E-03
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity 		0 1 0 0 1 3.7E-03