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: C0278883
Disease: Metastatic melanoma
Metastatic melanoma
55 15 11 0.11 0 0 0
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
26 3 6 8.1E-02 0 0 0
Infiltrating duct carcinoma of female breast
21 5 5 7.1E-02 0 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
60 13 7 6.5E-02 0 0 0
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma
31 13 5 6.2E-02 0 0 0
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung
32 3 5 6.2E-02 0 0 0
Squamous cell carcinoma of the head and neck
7 2 3 5.2E-02 0 0 0
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
4 5 2 3.6E-02 0 0 0
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma
23 4 4 5.5E-02 1.0E-03 0 0
Conventional (Clear Cell) Renal Cell Carcinoma
19 6 3 4.3E-02 2.0E-03 0 0
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
41 23 4 4.4E-02 3.0E-03 0 0
CUI: C0796237
Disease: Mental Retardation, X-Linked 30
Mental Retardation, X-Linked 30
1 2 1 1.9E-02 9.0E-03 0 0
CUI: C0796249
Disease: Mental Retardation, X-Linked 47
Mental Retardation, X-Linked 47
1 2 1 1.9E-02 9.0E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
1 3 1 1.9E-02 1.1E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome
1 22 1 1.9E-02 1.1E-02 1 1.7E-02 5.0E-03
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2
1 1 1 1.9E-02 1.1E-02 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy
1 2 1 1.9E-02 1.1E-02 0 0
Familial medullary thyroid carcinoma
1 23 1 1.9E-02 1.1E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
1 2 1 1.9E-02 1.1E-02 0 0
Robinow syndrome, autosomal recessive
1 2 1 1.9E-02 1.1E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
1 5 1 1.9E-02 1.1E-02 0 0
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
1 1 1 1.9E-02 1.1E-02 0 0
Hereditary Myopathy with Early Respiratory Failure
1 1 1 1.9E-02 1.1E-02 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome
1 1 1 1.9E-02 1.1E-02 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome
1 1 1 1.9E-02 1.1E-02 0 0