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: C4551635
Disease: Deuteranopia
Deuteranopia 		3 0 3 0.75 0 0
CUI: C2931753
Disease: Achromatopsia incomplete, X-linked
Achromatopsia incomplete, X-linked 		2 0 2 0.50 0 0
CUI: C3887937
Disease: CONE DYSTROPHY 5, X-LINKED
CONE DYSTROPHY 5, X-LINKED 		2 0 2 0.50 0 0
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		9 0 4 0.44 0 0
CUI: C1839612
Disease: MYOPIA 1, X-LINKED
MYOPIA 1, X-LINKED 		4 0 2 0.33 0 0
CUI: C0339530
Disease: Progressive cone-rod dystrophy
Progressive cone-rod dystrophy 		6 0 2 0.25 0 0
CUI: C3159311
Disease: BORNHOLM EYE DISEASE
BORNHOLM EYE DISEASE 		7 0 2 0.22 0 0
CUI: C0162279
Disease: Choroidal detachment
Choroidal detachment 		3 0 1 0.17 0 0
CUI: C0267926
Disease: Postoperative biliary stricture
Postoperative biliary stricture 		3 0 1 0.17 0 0
CUI: C0553686
Disease: Cerebral herniation
Cerebral herniation 		3 0 1 0.17 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 3 0.12 0 0
CUI: C0029128
Disease: Optic Disk Drusen
Optic Disk Drusen 		6 0 1 0.11 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 0 2 0.11 0 0
CUI: C1719497
Disease: Localized chronic periodontitis
Localized chronic periodontitis 		6 0 1 0.11 0 0
CUI: C0003081
Disease: Anisometropia
Anisometropia 		7 0 1 1.0E-01 0 0
CUI: C0748351
Disease: respiratory compensation
respiratory compensation 		7 0 1 1.0E-01 0 0
CUI: C0242338
Disease: HTLV Infections
HTLV Infections 		8 0 1 9.1E-02 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 1 9.1E-02 0 0
CUI: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		8 0 1 9.1E-02 0 0
CUI: C4086945
Disease: Ventilatory Threshold
Ventilatory Threshold 		10 0 1 7.7E-02 0 0
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 2 7.4E-02 0 0
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		25 0 2 7.4E-02 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		12 0 1 6.7E-02 0 0
CUI: C3826394
Disease: Epilepsy in children
Epilepsy in children 		12 0 1 6.7E-02 0 0
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		12 0 1 6.7E-02 0 0