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: C0155003
Disease: Blindness, Transient
Blindness, Transient 		3 0 1 0.33 0 0
CUI: C0155359
Disease: Scleral staphyloma
Scleral staphyloma 		3 0 1 0.33 0 0
CUI: C0221473
Disease: Blindness, Hysterical
Blindness, Hysterical 		3 0 1 0.33 0 0
CUI: C0339730
Disease: Blindness, Acquired
Blindness, Acquired 		3 0 1 0.33 0 0
CUI: C0376288
Disease: Amaurosis
Amaurosis 		3 0 1 0.33 0 0
CUI: C0750958
Disease: Blindness, Monocular
Blindness, Monocular 		4 0 1 0.25 0 0
CUI: C1879328
Disease: Blindness both eyes NOS (disorder)
Blindness both eyes NOS (disorder) 		7 0 1 0.14 0 0
CUI: C0271215
Disease: Blindness, Legal
Blindness, Legal 		10 0 1 1.0E-01 0 0
CUI: C1852767
Disease: Hereditary macular coloboma
Hereditary macular coloboma 		11 0 1 9.1E-02 0 0
CUI: C1858080
Disease: Retinal Dystrophy, Early Onset Severe
Retinal Dystrophy, Early Onset Severe 		14 0 1 7.1E-02 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 1 4.8E-02 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc 		26 0 1 3.8E-02 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 3.3E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 2.4E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 2.1E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 1.5E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 1 1.2E-02 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.2E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 109 1 1.2E-02 3 2.8E-02
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 1.2E-02 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 1 1.1E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.1E-02 0 0
CUI: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis 		112 0 1 8.9E-03 0 0
CUI: C3495676
Disease: Anorectal Malformations
Anorectal Malformations 		112 0 1 8.9E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 8.7E-03 0 0