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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.6E-02
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		0 1 0 0 1 3.6E-02
CUI: C0151281
Disease: Genital ulcers
Genital ulcers 		0 6 0 0 1 3.0E-02
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration 		0 1 0 0 1 3.6E-02
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		0 1 0 0 1 3.6E-02
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		0 1 0 0 1 3.6E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 3.6E-02
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		0 1 0 0 1 3.6E-02
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		0 1 0 0 1 3.6E-02
CUI: C0744669
Disease: Complex congenital heart disease
Complex congenital heart disease 		0 1 0 0 1 3.6E-02
CUI: C0750145
Disease: Occlusive vascular disease
Occlusive vascular disease 		0 1 0 0 1 3.6E-02
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		0 1 0 0 1 3.6E-02
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		0 1 0 0 1 3.6E-02
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		0 2 0 0 1 3.4E-02
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		0 2 0 0 1 3.4E-02
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		0 9 0 0 1 2.8E-02
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 9.5E-03
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		0 4 0 0 1 3.2E-02
CUI: C2217040
Disease: malignant neoplasm of large intestine stage IV
malignant neoplasm of large intestine stage IV 		0 1 0 0 1 3.6E-02
CUI: C2674574
Disease: Aortic aneurysm, familial thoracic 3
Aortic aneurysm, familial thoracic 3 		0 26 0 0 1 1.9E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.6E-02
CUI: C3536740
Disease: Cervical meningomyelocele
Cervical meningomyelocele 		0 1 0 0 1 3.6E-02
CUI: C3540094
Disease: INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		0 1 0 0 1 3.6E-02
CUI: C3553493
Disease: SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		0 1 0 0 1 3.6E-02
CUI: C3825293
Disease: Headache in children
Headache in children 		0 1 0 0 1 3.6E-02