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: C0302892
Disease: Congenital porencephaly
Congenital porencephaly 		9 3 9 1.00 3 1.00
CUI: C1854013
Disease: Anisomastia
Anisomastia 		4 0 3 0.30 0 0
CUI: C2895223
Disease: Juvenile and adolescent idiopathic scoliosis
Juvenile and adolescent idiopathic scoliosis 		4 0 3 0.30 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		34 3 9 0.26 3 1.00
CUI: C1867983
Disease: PORENCEPHALY, FAMILIAL
PORENCEPHALY, FAMILIAL 		2 0 2 0.22 0 0
CUI: C3281105
Disease: HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO
HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO 		2 0 2 0.22 0 0
CUI: C3698507
Disease: Post-traumatic Porencephaly
Post-traumatic Porencephaly 		2 0 2 0.22 0 0
CUI: C4082301
Disease: Developmental Porencephaly
Developmental Porencephaly 		2 0 2 0.22 0 0
CUI: C4551998
Disease: Porencephaly, Type 1, Autosomal Dominant
Porencephaly, Type 1, Autosomal Dominant 		2 15 2 0.22 1 5.9E-02
CUI: C2673195
Disease: Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps 		3 18 2 0.20 1 5.0E-02
CUI: C2986622
Disease: Cervical Intraepithelial Neoplasia Grade 2/3
Cervical Intraepithelial Neoplasia Grade 2/3 		9 0 3 0.20 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 2 0.20 0 0
CUI: C0740418
Disease: Chronic back pain
Chronic back pain 		10 0 3 0.19 0 0
CUI: C1298685
Disease: Chronic pain syndrome
Chronic pain syndrome 		10 0 3 0.19 0 0
CUI: C2051831
Disease: Pectus excavatum
Pectus excavatum 		12 0 3 0.17 0 0
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		6 0 2 0.15 0 0
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		7 0 2 0.14 0 0
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis 		17 0 3 0.13 0 0
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		9 0 2 0.12 0 0
CUI: C0266484
Disease: Schizencephaly
Schizencephaly 		10 0 2 0.12 0 0
CUI: C0425913
Disease: Uterus absent (finding)
Uterus absent (finding) 		10 0 2 0.12 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 0.11 0 0
CUI: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias 		1 0 1 0.11 0 0
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion 		1 0 1 0.11 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		1 0 1 0.11 0 0