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: C0854051
Disease: Allergy to sting
Allergy to sting 		1 0 1 9.1E-02 0 0
CUI: C0854771
Disease: Stage I Esophageal Squamous Cell Carcinoma
Stage I Esophageal Squamous Cell Carcinoma 		1 0 1 9.1E-02 0 0
CUI: C0857172
Disease: Persistent dry cough
Persistent dry cough 		1 0 1 9.1E-02 0 0
CUI: C0865262
Disease: Thrombopathy
Thrombopathy 		1 0 1 9.1E-02 0 0
CUI: C0877456
Disease: Heyde's syndrome
Heyde's syndrome 		1 0 1 9.1E-02 0 0
CUI: C0877603
Disease: Anteroseptal infarction
Anteroseptal infarction 		1 0 1 9.1E-02 0 0
CUI: C1112473
Disease: Mast cell aggregation
Mast cell aggregation 		1 0 1 9.1E-02 0 0
CUI: C1168329
Disease: Flash pulmonary oedema
Flash pulmonary oedema 		1 0 1 9.1E-02 0 0
CUI: C1265792
Disease: Chronic emphysema
Chronic emphysema 		1 0 1 9.1E-02 0 0
CUI: C1848525
Disease: von Willebrand Disease, Recessive Form
von Willebrand Disease, Recessive Form 		1 0 1 9.1E-02 0 0
CUI: C1862874
Disease: ANGIOTENSIN I-CONVERTING ENZYME, BENIGN SERUM INCREASE
ANGIOTENSIN I-CONVERTING ENZYME, BENIGN SERUM INCREASE 		1 0 1 9.1E-02 0 0
CUI: C1865241
Disease: Large sternal ossification centers
Large sternal ossification centers 		1 0 1 9.1E-02 0 0
CUI: C1865254
Disease: Distal widening of metacarpals
Distal widening of metacarpals 		1 0 1 9.1E-02 0 0
CUI: C2349195
Disease: Acute Anterior Wall Myocardial Infarction
Acute Anterior Wall Myocardial Infarction 		1 0 1 9.1E-02 0 0
CUI: C2584777
Disease: Autoimmune thrombotic thrombocytopenic purpura
Autoimmune thrombotic thrombocytopenic purpura 		1 0 1 9.1E-02 0 0
CUI: C2675470
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 9.1E-02 0 0
CUI: C2675525
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C2875367
Disease: Complex regional pain syndrome I, unspecified
Complex regional pain syndrome I, unspecified 		1 0 1 9.1E-02 0 0
CUI: C3151036
Disease: CHROMOSOME 1p32-p31 DELETION SYNDROME
CHROMOSOME 1p32-p31 DELETION SYNDROME 		1 0 1 9.1E-02 0 0
CUI: C3275121
Disease: One Vessel Coronary Disease
One Vessel Coronary Disease 		1 0 1 9.1E-02 0 0
CUI: C3640053
Disease: Renal Artery Disease
Renal Artery Disease 		1 0 1 9.1E-02 0 0
CUI: C3888796
Disease: Intestinal angioedema
Intestinal angioedema 		1 0 1 9.1E-02 0 0
CUI: C4017296
Disease: VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO
VON WILLEBRAND DISEASE, TYPE 1, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C4017650
Disease: VON WILLEBRAND FACTOR VICENZA PHENOTYPE
VON WILLEBRAND FACTOR VICENZA PHENOTYPE 		1 0 1 9.1E-02 0 0
CUI: C4024187
Disease: Bullet-shaped middle phalanges of the hand
Bullet-shaped middle phalanges of the hand 		1 0 1 9.1E-02 0 0