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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 5.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.7E-03
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 5.7E-03
CUI: C0442840
Disease: Cardiac embolism
Cardiac embolism 		0 3 0 0 1 5.6E-03
CUI: C0549117
Disease: Frontal lobe syndrome
Frontal lobe syndrome 		0 3 0 0 1 5.6E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 5.6E-03
CUI: C1336970
Disease: Visual Manifestations
Visual Manifestations 		0 1 0 0 1 5.7E-03
CUI: C1405458
Disease: Language Problems
Language Problems 		0 2 0 0 1 5.6E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 5.4E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 5.7E-03
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 5.7E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 5.7E-03
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 5.7E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 5.7E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 3 1.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.7E-03
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 5.7E-03
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 5.6E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 5.7E-03
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 1.1E-03 0 0
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		67 0 1 1.1E-03 0 0
CUI: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		65 0 1 1.1E-03 0 0
CUI: C0426817
Disease: Short ribs
Short ribs 		60 0 1 1.1E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.1E-03 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 1 1.2E-03 0 0