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: C0392775
Disease: Cystic medial necrosis of aorta
Cystic medial necrosis of aorta 		2 0 1 0.20 0 0
CUI: C0995195
Disease: Anoxia of brain
Anoxia of brain 		2 0 1 0.20 0 0
CUI: C1140716
Disease: Hypoxic Brain Damage
Hypoxic Brain Damage 		2 0 1 0.20 0 0
CUI: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary 		2 0 1 0.20 0 0
CUI: C1846837
Disease: Aortic Aneurysm, Familial Thoracic 2
Aortic Aneurysm, Familial Thoracic 2 		2 0 1 0.20 0 0
CUI: C1850993
Disease: Foveal Hypoplasia, Isolated
Foveal Hypoplasia, Isolated 		2 0 1 0.20 0 0
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO 		2 0 1 0.20 0 0
CUI: C3805604
Disease: FOVEAL HYPOPLASIA 1
FOVEAL HYPOPLASIA 1 		2 0 1 0.20 0 0
CUI: C4022524
Disease: Hypoplastic anterior commissure
Hypoplastic anterior commissure 		2 0 1 0.20 0 0
CUI: C4024811
Disease: Peripheral vitreous opacities
Peripheral vitreous opacities 		2 0 1 0.20 0 0
CUI: C4024960
Disease: Unilateral polymicrogyria
Unilateral polymicrogyria 		2 0 1 0.20 0 0
CUI: C4073008
Disease: Abnormal best corrected visual acuity test
Abnormal best corrected visual acuity test 		2 0 1 0.20 0 0
CUI: C4289994
Disease: Adenosine Deaminase 2 Deficiency
Adenosine Deaminase 2 Deficiency 		2 0 1 0.20 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 1 0.20 0 0
CUI: C4703595
Disease: Increased proinsulin:insulin ratio
Increased proinsulin:insulin ratio 		2 0 1 0.20 0 0
CUI: C0155118
Disease: Corneal degeneration
Corneal degeneration 		3 0 1 0.17 0 0
CUI: C0271135
Disease: Ectopic pupil
Ectopic pupil 		3 0 1 0.17 0 0
CUI: C0344543
Disease: Aniridia type 2
Aniridia type 2 		3 0 1 0.17 0 0
CUI: C0549307
Disease: Morning glory syndrome
Morning glory syndrome 		3 0 1 0.17 0 0
CUI: C1833797
Disease: Optic Nerve Hypoplasia, Bilateral
Optic Nerve Hypoplasia, Bilateral 		3 0 1 0.17 0 0
CUI: C2673186
Disease: Aortic Aneurysm, Familial Thoracic 6
Aortic Aneurysm, Familial Thoracic 6 		3 0 1 0.17 0 0
CUI: C2919194
Disease: Sporadic olivopontocerebellar atrophy
Sporadic olivopontocerebellar atrophy 		3 0 1 0.17 0 0
CUI: C2931803
Disease: Deletion 11p13
Deletion 11p13 		3 0 1 0.17 0 0
CUI: C3279690
Disease: MOYAMOYA DISEASE 5
MOYAMOYA DISEASE 5 		3 0 1 0.17 0 0
CUI: C3281027
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7 		3 0 1 0.17 0 0