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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 2.6E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.8E-02
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric 		0 4 0 0 1 2.6E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 2.8E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.4E-02
CUI: C0339470
Disease: Visually threatening diabetic retinopathy
Visually threatening diabetic retinopathy 		0 4 0 0 1 2.6E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 6.3E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.8E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 2 3.6E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 2.7E-02
CUI: C2919365
Disease: Macroalbuminuric diabetic nephropathy
Macroalbuminuric diabetic nephropathy 		0 2 0 0 1 2.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 2.6E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 2 5.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.8E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.6E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 2 4.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.8E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 2.7E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 2.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 8.3E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 1 1.5E-03 0 0
CUI: C0027092
Disease: Myopia
Myopia 		490 0 1 1.8E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index 		1014 0 2 1.9E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 1 2.0E-03 0 0