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: C0262361
Disease: Growth abnormality
Growth abnormality 		49 0 1 1.1E-03 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 1.1E-03 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		48 0 1 1.1E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 1.1E-03 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 1.1E-03 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 1.1E-03 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 1.1E-03 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput 		45 0 1 1.1E-03 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 0 1 1.1E-03 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 1 1.1E-03 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 1.1E-03 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 1 1.1E-03 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 1 1.1E-03 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 1.1E-03 0 0
CUI: C0426818
Disease: Thin rib
Thin rib 		42 0 1 1.1E-03 0 0
CUI: C4021792
Disease: Abnormality of the clavicle
Abnormality of the clavicle 		42 0 1 1.1E-03 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 1 1.1E-03 0 0
CUI: C0162292
Disease: External Ophthalmoplegia
External Ophthalmoplegia 		41 0 1 1.1E-03 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 0 1 1.1E-03 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 1.1E-03 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 1.1E-03 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		41 0 1 1.1E-03 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 1.1E-03 0 0
CUI: C1285654
Disease: Memory performance
Memory performance 		40 0 1 1.1E-03 0 0
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 1.1E-03 0 0