Source: CURATED ×
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: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		104 0 71 0.29 0 0
CUI: C4277690
Disease: Ciliopathies
Ciliopathies 		110 0 62 0.24 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		117 0 36 0.12 0 0
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2 		29 0 20 9.0E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		22 0 17 7.8E-02 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		17 0 16 7.5E-02 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		17 0 15 7.0E-02 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment 		98 0 17 5.8E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		30 0 13 5.7E-02 0 0
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		13 0 12 5.6E-02 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		12 0 11 5.2E-02 0 0
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		12 0 11 5.2E-02 0 0
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		12 0 11 5.2E-02 0 0
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		12 0 11 5.2E-02 0 0
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		12 0 11 5.2E-02 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		12 0 11 5.2E-02 0 0
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		21 0 11 5.0E-02 0 0
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 		13 0 10 4.7E-02 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		18 0 10 4.5E-02 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		15 0 9 4.1E-02 0 0
CUI: C4551568
Disease: Joubert syndrome 1
Joubert syndrome 1 		21 0 9 4.0E-02 0 0
CUI: C0028754
Disease: Obesity
Obesity 		205 0 15 3.7E-02 0 0
CUI: C3540662
Disease: Congenital Amaurosis of Retinal Origin
Congenital Amaurosis of Retinal Origin 		8 0 7 3.3E-02 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		12 0 7 3.2E-02 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		81 0 9 3.2E-02 0 0