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: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 2 8.3E-02 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 2 8.3E-02 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 3 8.3E-02 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		13 0 2 8.0E-02 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		13 0 2 8.0E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 7 7.8E-02 0 0
CUI: C1858080
Disease: Retinal Dystrophy, Early Onset Severe
Retinal Dystrophy, Early Onset Severe 		14 0 2 7.7E-02 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		14 0 2 7.7E-02 0 0
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		1 0 1 7.1E-02 0 0
CUI: C0339541
Disease: Goldmann-Favre syndrome (disorder)
Goldmann-Favre syndrome (disorder) 		1 2 1 7.1E-02 1 4.5E-02
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 3 7.1E-02 0 0
CUI: C1744705
Disease: Atrophy of optic disc
Atrophy of optic disc 		1 0 1 7.1E-02 0 0
CUI: C1834330
Disease: Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type
Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type 		1 0 1 7.1E-02 0 0
CUI: C1845407
Disease: CONE-ROD DYSTROPHY, X-LINKED, 3
CONE-ROD DYSTROPHY, X-LINKED, 3 		1 0 1 7.1E-02 0 0
CUI: C1970163
Disease: RETINITIS PIGMENTOSA 37 (disorder)
RETINITIS PIGMENTOSA 37 (disorder) 		1 6 1 7.1E-02 3 0.12
CUI: C2932677
Disease: Idiopathic Juxtafoveal Retinal Telangiectasia
Idiopathic Juxtafoveal Retinal Telangiectasia 		1 0 1 7.1E-02 0 0
CUI: C3150678
Disease: OGUCHI DISEASE 2
OGUCHI DISEASE 2 		1 0 1 7.1E-02 0 0
CUI: C3151086
Disease: Retinitis Pigmentosa 20
Retinitis Pigmentosa 20 		1 0 1 7.1E-02 0 0
CUI: C4016457
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE 		1 0 1 7.1E-02 0 0
CUI: C4072868
Disease: Paravenous chorioretinal atrophy
Paravenous chorioretinal atrophy 		1 0 1 7.1E-02 0 0
CUI: C4072995
Disease: Difficulty adjusting from light to dark
Difficulty adjusting from light to dark 		1 0 1 7.1E-02 0 0
CUI: C4274354
Disease: Severe early childhood onset retinal dystrophy
Severe early childhood onset retinal dystrophy 		1 0 1 7.1E-02 0 0
CUI: C4707246
Disease: Biallelic RPE65 mutation associated retinal dystrophy
Biallelic RPE65 mutation associated retinal dystrophy 		1 0 1 7.1E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 4 6.9E-02 0 0
CUI: C3888198
Disease: BESTROPHINOPATHY, AUTOSOMAL RECESSIVE
BESTROPHINOPATHY, AUTOSOMAL RECESSIVE 		17 0 2 6.9E-02 0 0