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 2.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.5E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 2.5E-02
CUI: C0266427
Disease: Testicular regression syndrome
Testicular regression syndrome 		0 3 0 0 1 2.4E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.2E-02
CUI: C0339470
Disease: Visually threatening diabetic retinopathy
Visually threatening diabetic retinopathy 		0 4 0 0 1 2.3E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 2.4E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.4E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon 		0 1 0 0 1 2.5E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 2.5E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.5E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 2.5E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 2.1E-02
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 2.3E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 78 1 2.7E-03 1 8.5E-03
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.9E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 3.0E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 3.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.1E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 3.1E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 3.2E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.2E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 3.3E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 3.3E-03 0 0