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: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 0.33 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 1 1 0.33 1 0.20
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		1 1 1 0.33 1 0.20
CUI: C0271574
Disease: Empty Sella Syndrome, Primary
Empty Sella Syndrome, Primary 		1 0 1 0.33 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		1 1 1 0.33 1 0.20
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		1 1 1 0.33 1 0.20
CUI: C0751097
Disease: Empty Sella Syndrome, Secondary
Empty Sella Syndrome, Secondary 		1 0 1 0.33 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		1 1 1 0.33 1 0.20
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		1 1 1 0.33 1 0.20
CUI: C1291575
Disease: Deficiency of citrate(si)-synthase
Deficiency of citrate(si)-synthase 		1 0 1 0.33 0 0
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		1 2 1 0.33 1 0.17
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.33 0 0
CUI: C2217040
Disease: malignant neoplasm of large intestine stage IV
malignant neoplasm of large intestine stage IV 		1 1 1 0.33 1 0.20
CUI: C3280099
Disease: CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME 		1 0 1 0.33 0 0
CUI: C3536740
Disease: Cervical meningomyelocele
Cervical meningomyelocele 		1 1 1 0.33 1 0.20
CUI: C3825293
Disease: Headache in children
Headache in children 		1 1 1 0.33 1 0.20
CUI: C4017062
Disease: HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY 		1 0 1 0.33 0 0
CUI: C4023332
Disease: Abnormal corneal endothelium morphology
Abnormal corneal endothelium morphology 		1 0 1 0.33 0 0
CUI: C4302205
Disease: Neonatal thrombosis of cerebral venous sinus
Neonatal thrombosis of cerebral venous sinus 		1 2 1 0.33 1 0.17
CUI: C4303479
Disease: Homocystinuria without methylmalonic aciduria
Homocystinuria without methylmalonic aciduria 		1 0 1 0.33 0 0
CUI: C4525128
Disease: Stage IV Colon Cancer AJCC v8
Stage IV Colon Cancer AJCC v8 		1 1 1 0.33 1 0.20
CUI: C4540434
Disease: COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA
COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA 		1 0 1 0.33 0 0
CUI: C1960883
Disease: Spina bifida aperta of cervical spine
Spina bifida aperta of cervical spine 		6 0 2 0.29 0 0
CUI: C0010035
Disease: Hereditary corneal dystrophy
Hereditary corneal dystrophy 		2 0 1 0.25 0 0
CUI: C0014670
Disease: Equinus Deformity
Equinus Deformity 		2 0 1 0.25 0 0