Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Infiltrating duct carcinoma of female breast
21 0 6 0.11 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
54 0 8 9.2E-02 0 0
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma
23 0 5 8.5E-02 0 0
CUI: C0278883
Disease: Metastatic melanoma
Metastatic melanoma
54 0 7 8.0E-02 0 0
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma
31 0 5 7.5E-02 0 0
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung
32 0 5 7.4E-02 0 0
Conventional (Clear Cell) Renal Cell Carcinoma
19 0 4 7.1E-02 0 0
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
54 0 4 4.4E-02 0 0
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
31 0 3 4.3E-02 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
1 0 1 2.4E-02 0 0
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
1 0 1 2.4E-02 0 0
CUI: C0265252
Disease: Coffin-Lowry syndrome
Coffin-Lowry syndrome
1 0 1 2.4E-02 0 0
CUI: C0265344
Disease: Donohue Syndrome
Donohue Syndrome
1 0 1 2.4E-02 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome
1 0 1 2.4E-02 0 0
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
1 0 1 2.4E-02 0 0
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
1 0 1 2.4E-02 0 0
CUI: C0796225
Disease: Mental Retardation, X-Linked 19
Mental Retardation, X-Linked 19
1 0 1 2.4E-02 0 0
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative
1 0 1 2.4E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
1 0 1 2.4E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
1 0 1 2.4E-02 0 0
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
1 0 1 2.4E-02 0 0
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
1 0 1 2.4E-02 0 0
CUI: C1861825
Disease: CATARACT, POSTERIOR POLAR, 1
CATARACT, POSTERIOR POLAR, 1
1 0 1 2.4E-02 0 0
Hereditary Myopathy with Early Respiratory Failure
1 0 1 2.4E-02 0 0
Hyperinsulinemic Hypoglycemia, Familial, 5
1 0 1 2.4E-02 0 0