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: C0005744
Disease: Blepharophimosis
Blepharophimosis
106 0 1 8.8E-03 0 0
CUI: C0005967
Disease: Bone neoplasms
Bone neoplasms
151 0 1 6.3E-03 0 0
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder
221 0 1 4.4E-03 0 0
CUI: C0006111
Disease: Brain Diseases
Brain Diseases
345 0 1 2.8E-03 0 0
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
1018 0 1 9.8E-04 0 0
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
556 0 1 1.8E-03 0 0
CUI: C0007095
Disease: Carcinoid Tumor
Carcinoid Tumor
267 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: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
508 0 1 1.9E-03 0 0
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
949 0 1 1.0E-03 0 0
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
108 0 1 8.7E-03 0 0
CUI: C0007129
Disease: Merkel cell carcinoma
Merkel cell carcinoma
226 0 1 4.3E-03 0 0
CUI: C0007138
Disease: Carcinoma, Transitional Cell
Carcinoma, Transitional Cell
623 0 1 1.6E-03 0 0
CUI: C0007642
Disease: Cellulitis
Cellulitis
38 0 1 2.2E-02 0 0
CUI: C0007682
Disease: CNS disorder
CNS disorder
319 0 1 3.1E-03 0 0
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
687 0 1 1.4E-03 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence
1 0 1 0.12 0 0
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
140 0 1 6.8E-03 0 0
CUI: C0008031
Disease: Chest Pain
Chest Pain
154 0 1 6.2E-03 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities
355 0 1 2.8E-03 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis
420 0 1 2.3E-03 0 0
CUI: C0008479
Disease: Chondrosarcoma
Chondrosarcoma
385 0 1 2.6E-03 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
757 0 1 1.3E-03 0 0
CUI: C0008732
Disease: Chylous Ascites
Chylous Ascites
6 0 1 7.7E-02 0 0