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: C0001916
Disease: Albinism
Albinism 		0 27 0 0 1 6.1E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 6.8E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 7.2E-03
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		0 1 0 0 1 7.2E-03
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		0 5 0 0 1 7.0E-03
CUI: C0236792
Disease: Asperger Syndrome
Asperger Syndrome 		0 3 0 0 1 7.1E-03
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		0 1 0 0 1 7.2E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 7.2E-03
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		0 1 0 0 1 7.2E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 7.2E-03
CUI: C0334328
Disease: Microfollicular adenoma
Microfollicular adenoma 		0 1 0 0 1 7.2E-03
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		0 1 0 0 1 7.2E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 7.0E-03
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle 		0 1 0 0 1 7.2E-03
CUI: C0345906
Disease: Sarcoma of liver
Sarcoma of liver 		0 1 0 0 1 7.2E-03
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		0 1 0 0 1 7.2E-03
CUI: C0522254
Disease: Analgesic Overuse Headache
Analgesic Overuse Headache 		0 9 0 0 1 6.8E-03
CUI: C0750145
Disease: Occlusive vascular disease
Occlusive vascular disease 		0 1 0 0 1 7.2E-03
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		0 1 0 0 1 7.2E-03
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		0 1 0 0 1 7.2E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 7.2E-03
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		0 2 0 0 1 7.2E-03
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		0 2 0 0 1 7.2E-03
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		0 9 0 0 1 6.8E-03
CUI: C1856058
Disease: HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY 		0 78 0 0 1 4.7E-03