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: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		13 24 5 0.14 2 3.2E-02
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 8 0.13 0 0
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
Melanocortin 4 Receptor Deficiency 		24 28 6 0.13 3 4.5E-02
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 8 0.13 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 31 11 0.11 1 1.4E-02
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 3 11 0.10 1 2.3E-02
CUI: C1836926
Disease: Bone spicule pigmentation of the retina
Bone spicule pigmentation of the retina 		24 0 5 0.10 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 16 9.4E-02 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 11 9.2E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 74 8 9.0E-02 3 2.7E-02
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 227 20 8.8E-02 1 3.7E-03
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 4 8.7E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 9 8.5E-02 1 1.1E-02
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity 		11 4 3 8.1E-02 1 2.3E-02
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc 		26 0 4 7.8E-02 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 16 7.7E-02 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 3 7.7E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 1 6 7.5E-02 1 2.4E-02
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 2 3 7.5E-02 1 2.4E-02
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 3 7.5E-02 0 0
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 		86 163 8 7.5E-02 3 1.5E-02
CUI: C1839025
Disease: Decreased light- and dark-adapted electroretinogram amplitude
Decreased light- and dark-adapted electroretinogram amplitude 		15 0 3 7.3E-02 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 3 7.1E-02 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 3 7.1E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 18 13 7.1E-02 3 5.4E-02