Source: ALL
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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		5473 0 1 1.8E-04 0 0
CUI: C0011847
Disease: Diabetes
Diabetes 		2359 0 1 4.2E-04 0 0
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		2803 0 1 3.6E-04 0 0
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		522 0 1 1.9E-03 0 0
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		645 0 1 1.6E-03 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		400 0 1 2.5E-03 0 0
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		3806 0 1 2.6E-04 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms 		10161 0 1 9.8E-05 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 6.0E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 0 1 1.2E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		546 0 1 1.8E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		716 0 1 1.4E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 6.8E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia 		184 0 1 5.4E-03 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 1 3.1E-02 0 0
CUI: C0456909
Disease: Blindness
Blindness 		393 0 1 2.5E-03 0 0
CUI: C0494165
Disease: Secondary malignant neoplasm of liver
Secondary malignant neoplasm of liver 		951 0 1 1.1E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 1.0E-02 0 0
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		3720 0 1 2.7E-04 0 0
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		6626 0 1 1.5E-04 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 1 3.2E-02 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 1 3.8E-02 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 1 8.3E-02 0 0
CUI: C1854065
Disease: LATE-ONSET RETINAL DEGENERATION (disorder)
LATE-ONSET RETINAL DEGENERATION (disorder) 		17 0 1 5.9E-02 0 0
CUI: C1864870
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		1 0 1 1.00 0 0