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: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		1 0 1 4.2E-02 0 0
CUI: C0233737
Disease: Circumlocution
Circumlocution 		1 0 1 4.2E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy 		1 0 1 4.2E-02 0 0
CUI: C1419614
Disease: RETINITIS PIGMENTOSA 28
RETINITIS PIGMENTOSA 28 		1 0 1 4.2E-02 0 0
CUI: C1531646
Disease: Central topographic island
Central topographic island 		1 0 1 4.2E-02 0 0
CUI: C1836006
Disease: NANOPHTHALMOS 2 (disorder)
NANOPHTHALMOS 2 (disorder) 		1 0 1 4.2E-02 0 0
CUI: C1836916
Disease: POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA 		1 0 1 4.2E-02 0 0
CUI: C1838601
Disease: Retinitis Pigmentosa 11
Retinitis Pigmentosa 11 		1 0 1 4.2E-02 0 0
CUI: C1840284
Disease: LEBER CONGENITAL AMAUROSIS 11
LEBER CONGENITAL AMAUROSIS 11 		1 0 1 4.2E-02 0 0
CUI: C1842816
Disease: RETINITIS PIGMENTOSA 30
RETINITIS PIGMENTOSA 30 		1 0 1 4.2E-02 0 0
CUI: C1854061
Disease: Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 		1 0 1 4.2E-02 0 0
CUI: C1859566
Disease: BARDET-BIEDL SYNDROME 8
BARDET-BIEDL SYNDROME 8 		1 0 1 4.2E-02 0 0
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		1 0 1 4.2E-02 0 0
CUI: C1866422
Disease: RETINITIS PIGMENTOSA 19
RETINITIS PIGMENTOSA 19 		1 0 1 4.2E-02 0 0
CUI: C1970236
Disease: Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen
Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen 		1 0 1 4.2E-02 0 0
CUI: C1970573
Disease: MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO 		1 0 1 4.2E-02 0 0
CUI: C2674407
Disease: Foveoschisis
Foveoschisis 		1 0 1 4.2E-02 0 0
CUI: C2932677
Disease: Idiopathic Juxtafoveal Retinal Telangiectasia
Idiopathic Juxtafoveal Retinal Telangiectasia 		1 0 1 4.2E-02 0 0
CUI: C3150691
Disease: RETINITIS PIGMENTOSA 54
RETINITIS PIGMENTOSA 54 		1 0 1 4.2E-02 0 0
CUI: C3150715
Disease: RETINITIS PIGMENTOSA 51
RETINITIS PIGMENTOSA 51 		1 0 1 4.2E-02 0 0
CUI: C3150879
Disease: RETINITIS PIGMENTOSA 58
RETINITIS PIGMENTOSA 58 		1 0 1 4.2E-02 0 0
CUI: C3151001
Disease: Retinitis Pigmentosa 4
Retinitis Pigmentosa 4 		1 0 1 4.2E-02 0 0
CUI: C3151138
Disease: RETINITIS PIGMENTOSA 39 (disorder)
RETINITIS PIGMENTOSA 39 (disorder) 		1 0 1 4.2E-02 0 0
CUI: C3151192
Disease: LEBER CONGENITAL AMAUROSIS 7
LEBER CONGENITAL AMAUROSIS 7 		1 0 1 4.2E-02 0 0
CUI: C3151206
Disease: LEBER CONGENITAL AMAUROSIS 15
LEBER CONGENITAL AMAUROSIS 15 		1 0 1 4.2E-02 0 0