Source: BEFREE ×
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 2.8E-03
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 2.8E-03
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration 		0 1 0 0 1 2.8E-03
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		0 4 0 0 2 5.6E-03
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		0 1 0 0 1 2.8E-03
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		0 1 0 0 1 2.8E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 2.8E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 2.8E-03
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		0 1 0 0 1 2.8E-03
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		0 1 0 0 1 2.8E-03
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		0 1 0 0 1 2.8E-03
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		0 1 0 0 1 2.8E-03
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein 		0 1 0 0 1 2.8E-03
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		0 2 0 0 1 2.8E-03
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		0 2 0 0 1 2.8E-03
CUI: C1845069
Disease: ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder) 		0 2 0 0 1 2.8E-03
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		0 1 0 0 1 2.8E-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 4 0 0 2 5.6E-03
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		0 4 0 0 2 5.6E-03
CUI: C1863198
Disease: ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder) 		0 2 0 0 1 2.8E-03
CUI: C2217040
Disease: malignant neoplasm of large intestine stage IV
malignant neoplasm of large intestine stage IV 		0 1 0 0 1 2.8E-03
CUI: C3536740
Disease: Cervical meningomyelocele
Cervical meningomyelocele 		0 1 0 0 1 2.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.8E-03
CUI: C3825293
Disease: Headache in children
Headache in children 		0 1 0 0 1 2.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.8E-03