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: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		5 0 2 0.13 0 0
CUI: C0021308
Disease: Infarction
Infarction 		15 0 3 0.12 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 2 0.12 0 0
CUI: C0338507
Disease: Non-arteritic ischemic optic neuropathy
Non-arteritic ischemic optic neuropathy 		6 0 2 0.12 0 0
CUI: C0340557
Disease: Atherosclerotic renal artery stenosis
Atherosclerotic renal artery stenosis 		6 0 2 0.12 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 2 0.12 0 0
CUI: C1960883
Disease: Spina bifida aperta of cervical spine
Spina bifida aperta of cervical spine 		6 0 2 0.12 0 0
CUI: C3647902
Disease: Vasculogenic erectile dysfunction
Vasculogenic erectile dysfunction 		6 0 2 0.12 0 0
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		52 0 7 0.12 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		16 0 3 0.12 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 2 0.12 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 2 0.12 0 0
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		7 0 2 0.12 0 0
CUI: C1852020
Disease: Malattia Leventinese
Malattia Leventinese 		7 0 2 0.12 0 0
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I 		7 0 2 0.12 0 0
CUI: C4055342
Disease: C3 Glomerulonephritis
C3 Glomerulonephritis 		7 0 2 0.12 0 0
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 3 0.12 0 0
CUI: C4477095
Disease: Increased lactate dehydrogenase activity
Increased lactate dehydrogenase activity 		27 0 4 0.11 0 0
CUI: C1299567
Disease: Neonatal stroke
Neonatal stroke 		8 0 2 0.11 0 0
CUI: C1866558
Disease: Neural tube defect, folate-sensitive
Neural tube defect, folate-sensitive 		8 0 2 0.11 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		9 0 2 0.11 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion 		9 0 2 0.11 0 0
CUI: C0155305
Disease: Optic Neuropathy, Ischemic
Optic Neuropathy, Ischemic 		9 0 2 0.11 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 0 2 0.11 0 0
CUI: C1832174
Disease: DOYNE HONEYCOMB RETINAL DYSTROPHY
DOYNE HONEYCOMB RETINAL DYSTROPHY 		9 0 2 0.11 0 0