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: C0005694
Disease: Bladder neck obstruction
Bladder neck obstruction
67 0 1 1.4E-02 0 0
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
2130 0 1 4.7E-04 0 0
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
267 0 1 3.7E-03 0 0
CUI: C0005866
Disease: Bluetongue infection
Bluetongue infection
13 0 1 5.9E-02 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.2E-04 0 0
CUI: C0005940
Disease: Bone Diseases
Bone Diseases
317 0 1 3.1E-03 0 0
CUI: C0005944
Disease: Metabolic Bone Disorder
Metabolic Bone Disorder
66 0 1 1.4E-02 0 0
CUI: C0005956
Disease: Bone Marrow Diseases
Bone Marrow Diseases
84 0 1 1.1E-02 0 0
CUI: C0005967
Disease: Bone neoplasms
Bone neoplasms
151 0 1 6.5E-03 0 0
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
556 0 1 1.8E-03 0 0
CUI: C0006625
Disease: Cachexia
Cachexia
273 0 1 3.6E-03 0 0
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
342 0 1 2.9E-03 0 0
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
472 0 1 2.1E-03 0 0
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
949 0 1 1.0E-03 0 0
Noninfiltrating Intraductal Carcinoma
486 0 1 2.0E-03 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
512 0 1 1.9E-03 0 0
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
1756 0 1 5.7E-04 0 0
CUI: C0007642
Disease: Cellulitis
Cellulitis
38 0 1 2.4E-02 0 0
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
311 0 1 3.2E-03 0 0
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
687 0 1 1.4E-03 0 0
CUI: C0008311
Disease: Cholangitis
Cholangitis
80 0 1 1.2E-02 0 0
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
478 0 1 2.1E-03 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis
420 0 1 2.4E-03 0 0
CUI: C0008449
Disease: Congenital anomaly of cartilage
Congenital anomaly of cartilage
9 0 1 7.7E-02 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
757 0 1 1.3E-03 0 0