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: C0035313
Disease: Retinal Dysplasia
Retinal Dysplasia 		34 2 20 0.12 1 9.1E-02
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 29 0.12 0 0
CUI: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy 		142 14 29 0.11 3 0.14
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 16 0.10 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 35 0.10 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		19 0 15 9.9E-02 0 0
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		21 0 15 9.7E-02 0 0
CUI: C4082144
Disease: Metatarsal Valgus
Metatarsal Valgus 		22 0 15 9.7E-02 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 23 9.7E-02 0 0
CUI: C0028840
Disease: Ocular Hypertension
Ocular Hypertension 		103 0 22 9.6E-02 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 17 9.6E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 23 9.6E-02 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia 		184 116 29 9.6E-02 1 8.0E-03
CUI: C0271055
Disease: Rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment 		47 0 17 9.6E-02 0 0
CUI: C1836373
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K 		14 0 14 9.5E-02 0 0
CUI: C4284790
Disease: Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 		14 0 14 9.5E-02 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 14 9.4E-02 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level 		16 0 14 9.3E-02 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos 		89 0 20 9.2E-02 0 0
CUI: C4025773
Disease: Aplasia/Hypoplasia involving the skeletal musculature
Aplasia/Hypoplasia involving the skeletal musculature 		19 0 14 9.2E-02 0 0
CUI: C4073168
Disease: Abnormal lactate dehydrogenase activity
Abnormal lactate dehydrogenase activity 		19 0 14 9.2E-02 0 0
CUI: C0027092
Disease: Myopia
Myopia 		490 0 53 9.1E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		770 198 76 9.0E-02 1 4.8E-03
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		23 0 14 8.9E-02 0 0
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos 		60 0 17 8.9E-02 0 0