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: C0008412
Disease: Choline Deficiency
Choline Deficiency 		0 4 0 0 1 6.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 7.7E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.12
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 7.4E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 7.7E-02
CUI: C0424101
Disease: Inattention
Inattention 		0 22 0 0 1 2.9E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 4.0E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 6.7E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 7.7E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 7.7E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 7.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 3 0.23
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms 		13 0 1 1.0E-02 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 1.1E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 1 5.2E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 5.6E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 1.1E-02 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.1E-02 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 8.9E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		94 0 1 5.6E-03 0 0
CUI: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.2E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 9.6E-03 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		130 0 1 4.7E-03 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 1.2E-02 0 0