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: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 103 0.12 0 0
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
620 0 107 0.12 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
407 0 84 0.12 0 0
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
136 0 55 0.11 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 63 0.11 0 0
Sensorineural Hearing Loss (disorder)
783 0 117 0.11 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
86 53 48 0.11 1 1.5E-02
Autosomal recessive retinitis pigmentosa
82 0 46 0.11 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 79 0.11 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 45 0.10 0 0
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
254 51 60 0.10 1 1.6E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
645 0 93 9.8E-02 0 0
CUI: C0042798
Disease: Low Vision
Low Vision
157 51 49 9.6E-02 1 1.6E-02
Amaurosis congenita of Leber, type 1
81 0 42 9.6E-02 0 0
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
384 0 65 9.0E-02 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 48 9.0E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 36 8.9E-02 0 0
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
302 92 57 8.8E-02 2 1.9E-02
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 76 8.8E-02 0 0
CUI: C0042164
Disease: Uveitis
Uveitis
247 0 52 8.7E-02 0 0
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration
125 0 42 8.7E-02 0 0
Attenuation of retinal blood vessels
41 0 34 8.4E-02 0 0
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
211 49 47 8.3E-02 2 3.3E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
1180 0 120 8.2E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 39 8.2E-02 0 0