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: C1610621
Disease: Factor II mutation
Factor II mutation 		2 2 1 0.33 1 1.0E-01
CUI: C1842704
Disease: GAUCHER DISEASE, PERINATAL LETHAL
GAUCHER DISEASE, PERINATAL LETHAL 		2 0 1 0.33 0 0
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration 		3 1 1 0.25 1 0.11
CUI: C0342704
Disease: Deficiency of Cobalamin G
Deficiency of Cobalamin G 		3 0 1 0.25 0 0
CUI: C0523631
Disease: Folic acid measurement
Folic acid measurement 		3 0 1 0.25 0 0
CUI: C1866558
Disease: Neural tube defect, folate-sensitive
Neural tube defect, folate-sensitive 		8 0 2 0.25 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 1 0.25 0 0
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 5 1 0.25 1 7.7E-02
CUI: C0221165
Disease: Diplegia
Diplegia 		4 2 1 0.20 1 1.0E-01
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 1 0.20 0 0
CUI: C0277005
Disease: Opisthorchis viverrini Infection
Opisthorchis viverrini Infection 		4 0 1 0.20 0 0
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle 		4 1 1 0.20 1 0.11
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 1 0.20 0 0
CUI: C0751711
Disease: Anterior Ischemic Optic Neuropathy
Anterior Ischemic Optic Neuropathy 		4 0 1 0.20 0 0
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein 		4 1 1 0.20 1 0.11
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY 		4 0 1 0.20 0 0
CUI: C3160733
Disease: THROMBOPHILIA DUE TO THROMBIN DEFECT
THROMBOPHILIA DUE TO THROMBIN DEFECT 		4 0 1 0.20 0 0
CUI: C3843752
Disease: Asthma, doctor diagnosed
Asthma, doctor diagnosed 		4 3 1 0.20 1 9.1E-02
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 2 0.18 0 0
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		5 1 1 0.17 1 0.11
CUI: C0086664
Disease: Myelocele
Myelocele 		5 0 1 0.17 0 0
CUI: C0158629
Disease: Congenital anomaly of aortic arch
Congenital anomaly of aortic arch 		5 0 1 0.17 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 1 0.17 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 1 0.17 0 0
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum 		12 0 2 0.17 0 0