Source: UNIPROT ×
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: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		54 0 11 0.11 0 0
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		41 0 7 8.0E-02 0 0
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		26 0 5 6.7E-02 0 0
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma 		31 0 5 6.2E-02 0 0
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung 		32 0 5 6.2E-02 0 0
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		23 0 4 5.5E-02 0 0
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		4 0 3 5.5E-02 0 0
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		31 0 4 4.9E-02 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		54 0 5 4.9E-02 0 0
CUI: C3165106
Disease: Infiltrating duct carcinoma of female breast
Infiltrating duct carcinoma of female breast 		21 0 3 4.2E-02 0 0
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		19 0 2 2.8E-02 0 0
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 0 1 1.9E-02 0 0
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		1 0 1 1.9E-02 0 0
CUI: C1704423
Disease: Milroy Disease
Milroy Disease 		1 0 1 1.9E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		1 0 1 1.9E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		1 0 1 1.9E-02 0 0
CUI: C1840390
Disease: Pseudohypoaldosteronism, Type IIb
Pseudohypoaldosteronism, Type IIb 		1 0 1 1.9E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		1 0 1 1.9E-02 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		1 0 1 1.9E-02 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		1 0 1 1.9E-02 0 0
CUI: C1866293
Disease: Retinal cone dystrophy 2
Retinal cone dystrophy 2 		1 0 1 1.9E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		1 0 1 1.9E-02 0 0
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		1 0 1 1.9E-02 0 0
CUI: C3552634
Disease: LYMPHOPROLIFERATIVE SYNDROME 1
LYMPHOPROLIFERATIVE SYNDROME 1 		1 0 1 1.9E-02 0 0
CUI: C3553270
Disease: DIARRHEA 6
DIARRHEA 6 		1 0 1 1.9E-02 0 0