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: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		1 0 1 0.17 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.17 0 0
CUI: C2217040
Disease: malignant neoplasm of large intestine stage IV
malignant neoplasm of large intestine stage IV 		1 0 1 0.17 0 0
CUI: C3536740
Disease: Cervical meningomyelocele
Cervical meningomyelocele 		1 0 1 0.17 0 0
CUI: C3810343
Disease: SACRAL AGENESIS WITH VERTEBRAL ANOMALIES
SACRAL AGENESIS WITH VERTEBRAL ANOMALIES 		1 0 1 0.17 0 0
CUI: C3825293
Disease: Headache in children
Headache in children 		1 0 1 0.17 0 0
CUI: C4017062
Disease: HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY 		1 0 1 0.17 0 0
CUI: C4302205
Disease: Neonatal thrombosis of cerebral venous sinus
Neonatal thrombosis of cerebral venous sinus 		1 0 1 0.17 0 0
CUI: C4303479
Disease: Homocystinuria without methylmalonic aciduria
Homocystinuria without methylmalonic aciduria 		1 0 1 0.17 0 0
CUI: C4525128
Disease: Stage IV Colon Cancer AJCC v8
Stage IV Colon Cancer AJCC v8 		1 0 1 0.17 0 0
CUI: C4540434
Disease: COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA
COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA 		1 0 1 0.17 0 0
CUI: C0152426
Disease: Craniorachischisis
Craniorachischisis 		38 0 6 0.16 0 0
CUI: C0080218
Disease: Tethered Cord Syndrome
Tethered Cord Syndrome 		41 0 6 0.15 0 0
CUI: C0014670
Disease: Equinus Deformity
Equinus Deformity 		2 0 1 0.14 0 0
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		2 0 1 0.14 0 0
CUI: C0343525
Disease: Lemierre Syndrome
Lemierre Syndrome 		2 0 1 0.14 0 0
CUI: C0427418
Disease: Folic acid measurement, RBC
Folic acid measurement, RBC 		2 0 1 0.14 0 0
CUI: C0431415
Disease: Lumbosacral agenesis
Lumbosacral agenesis 		2 0 1 0.14 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		2 0 1 0.14 0 0
CUI: C0751500
Disease: Petrous Sinus Thrombophlebitis
Petrous Sinus Thrombophlebitis 		2 0 1 0.14 0 0
CUI: C0751501
Disease: Intracranial Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitis 		2 0 1 0.14 0 0
CUI: C0751502
Disease: Petrous Sinus Thrombosis
Petrous Sinus Thrombosis 		2 0 1 0.14 0 0
CUI: C0812426
Disease: Kidney problem
Kidney problem 		2 0 1 0.14 0 0
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		2 0 1 0.14 0 0
CUI: C1838568
Disease: Sacral defect and anterior sacral meningocele
Sacral defect and anterior sacral meningocele 		2 0 1 0.14 0 0