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: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 0.14 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 0.14 0 0
CUI: C3280113
Disease: NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES 		1 10 1 0.14 6 0.35
CUI: C3489732
Disease: Familial mesangial sclerosis
Familial mesangial sclerosis 		1 0 1 0.14 0 0
CUI: C3501249
Disease: Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome
Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome 		1 0 1 0.14 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 0.14 0 0
CUI: C4476808
Disease: Microcoria
Microcoria 		1 0 1 0.14 0 0
CUI: C4748327
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		1 0 1 0.14 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 1 0.12 0 0
CUI: C0240017
Disease: Intercostal muscle weakness
Intercostal muscle weakness 		2 0 1 0.12 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 1 0.12 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 1 0.12 0 0
CUI: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 0 1 0.12 0 0
CUI: C4020790
Disease: Medullary sponge kidney disease
Medullary sponge kidney disease 		2 0 1 0.12 0 0
CUI: C4022580
Disease: Unfavorable response of muscle weakness to acetylcholine esterase inhibitors
Unfavorable response of muscle weakness to acetylcholine esterase inhibitors 		2 0 1 0.12 0 0
CUI: C0006902
Disease: Capillaritis
Capillaritis 		3 0 1 0.11 0 0
CUI: C0086588
Disease: Marasmus
Marasmus 		3 0 1 0.11 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 1 0.11 0 0
CUI: C0344263
Disease: Posterior lenticonus
Posterior lenticonus 		3 0 1 0.11 0 0
CUI: C1303009
Disease: Microcoria, congenital
Microcoria, congenital 		3 0 1 0.11 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 1 0.11 0 0
CUI: C1864238
Disease: Prolonged miniature endplate currents
Prolonged miniature endplate currents 		3 0 1 0.11 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 1 0.11 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 1 0.11 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 1 0.11 0 0