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: C0333494
Disease: Phlebosclerosis
Phlebosclerosis 		1 0 1 6.7E-02 0 0
CUI: C0549315
Disease: Hydatidiform mole, benign
Hydatidiform mole, benign 		1 0 1 6.7E-02 0 0
CUI: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 6.7E-02 0 0
CUI: C3280113
Disease: NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES 		1 0 1 6.7E-02 0 0
CUI: C3489732
Disease: Familial mesangial sclerosis
Familial mesangial sclerosis 		1 0 1 6.7E-02 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 6.7E-02 0 0
CUI: C3554634
Disease: Light complexion
Light complexion 		1 0 1 6.7E-02 0 0
CUI: C4225228
Disease: NEPHROTIC SYNDROME, TYPE 11
NEPHROTIC SYNDROME, TYPE 11 		1 0 1 6.7E-02 0 0
CUI: C4476808
Disease: Microcoria
Microcoria 		1 0 1 6.7E-02 0 0
CUI: C4538784
Disease: GALLOWAY-MOWAT SYNDROME 2, X-LINKED
GALLOWAY-MOWAT SYNDROME 2, X-LINKED 		1 0 1 6.7E-02 0 0
CUI: C4540266
Disease: GALLOWAY-MOWAT SYNDROME 3
GALLOWAY-MOWAT SYNDROME 3 		1 0 1 6.7E-02 0 0
CUI: C4540270
Disease: GALLOWAY-MOWAT SYNDROME 4
GALLOWAY-MOWAT SYNDROME 4 		1 0 1 6.7E-02 0 0
CUI: C4540274
Disease: GALLOWAY-MOWAT SYNDROME 5
GALLOWAY-MOWAT SYNDROME 5 		1 0 1 6.7E-02 0 0
CUI: C4748084
Disease: OVARIAN DYSGENESIS 6
OVARIAN DYSGENESIS 6 		1 0 1 6.7E-02 0 0
CUI: C4748549
Disease: NEPHROTIC SYNDROME, TYPE 18
NEPHROTIC SYNDROME, TYPE 18 		1 0 1 6.7E-02 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		2 0 1 6.2E-02 0 0
CUI: C1847114
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5 		2 0 2 0.13 0 0
CUI: C1855433
Disease: Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive
Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive 		2 0 1 6.2E-02 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 6.2E-02 0 0
CUI: C4551527
Disease: Focal segmental glomerulosclerosis 1
Focal segmental glomerulosclerosis 1 		2 0 1 6.2E-02 0 0
CUI: C0344263
Disease: Posterior lenticonus
Posterior lenticonus 		3 0 1 5.9E-02 0 0
CUI: C0451720
Disease: Nephrotic syndrome, focal and segmental glomerular lesions
Nephrotic syndrome, focal and segmental glomerular lesions 		3 0 1 5.9E-02 0 0
CUI: C1303009
Disease: Microcoria, congenital
Microcoria, congenital 		3 0 1 5.9E-02 0 0
CUI: C1864238
Disease: Prolonged miniature endplate currents
Prolonged miniature endplate currents 		3 0 1 5.9E-02 0 0
CUI: C2902887
Disease: Nephrotic syndrome with focal and segmental hyalinosis
Nephrotic syndrome with focal and segmental hyalinosis 		3 0 1 5.9E-02 0 0