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: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		0 6 0 0 1 2.6E-02
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 2.6E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 2.6E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 2.6E-03 0 0
CUI: C0022492
Disease: Kandinsky Syndrome
Kandinsky Syndrome 		1 0 1 2.6E-03 0 0
CUI: C0023213
Disease: Ventricular Outflow Obstruction, Left
Ventricular Outflow Obstruction, Left 		1 0 1 2.6E-03 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 2.6E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 2.6E-03 0 0
CUI: C0028313
Disease: Organic Brain Syndrome, Nonpsychotic
Organic Brain Syndrome, Nonpsychotic 		1 0 1 2.6E-03 0 0
CUI: C0029230
Disease: Organic Mental Disorders, Psychotic
Organic Mental Disorders, Psychotic 		1 0 1 2.6E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 2.6E-03 0 0
CUI: C0031946
Disease: Pinta
Pinta 		1 0 1 2.6E-03 0 0
CUI: C0033247
Disease: Proctocolitis
Proctocolitis 		1 0 1 2.6E-03 0 0
CUI: C0033943
Disease: Psychoses, Traumatic
Psychoses, Traumatic 		1 0 1 2.6E-03 0 0
CUI: C0035619
Disease: Ventricular Outflow Obstruction, Right
Ventricular Outflow Obstruction, Right 		1 0 1 2.6E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.6E-03 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 2.6E-03 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction 		1 0 1 2.6E-03 0 0
CUI: C0149877
Disease: Hypoglycemic encephalopathy
Hypoglycemic encephalopathy 		1 0 1 2.6E-03 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 2.6E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.6E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 2.6E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 2.6E-03 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis 		1 0 1 2.6E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 2.6E-03 0 0