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: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		4 0 4 0.40 0 0
CUI: C1867983
Disease: PORENCEPHALY, FAMILIAL
PORENCEPHALY, FAMILIAL 		2 0 2 0.20 0 0
CUI: C3281105
Disease: HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO
HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO 		2 0 2 0.20 0 0
CUI: C3698507
Disease: Post-traumatic Porencephaly
Post-traumatic Porencephaly 		2 0 2 0.20 0 0
CUI: C4082301
Disease: Developmental Porencephaly
Developmental Porencephaly 		2 0 2 0.20 0 0
CUI: C4551998
Disease: Porencephaly, Type 1, Autosomal Dominant
Porencephaly, Type 1, Autosomal Dominant 		2 0 2 0.20 0 0
CUI: C2673195
Disease: Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps 		3 0 2 0.18 0 0
CUI: C1840529
Disease: HOLOPROSENCEPHALY 3
HOLOPROSENCEPHALY 3 		4 0 2 0.17 0 0
CUI: C0685869
Disease: Monophthalmos
Monophthalmos 		6 0 2 0.14 0 0
CUI: C0302892
Disease: Congenital porencephaly
Congenital porencephaly 		9 0 2 0.12 0 0
CUI: C4082173
Disease: Porencephaly
Porencephaly 		9 0 2 0.12 0 0
CUI: C0266320
Disease: Impervious ureter
Impervious ureter 		1 0 1 1.0E-01 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 0 2 1.0E-01 0 0
CUI: C0599949
Disease: Arterial Stiffness
Arterial Stiffness 		1 0 1 1.0E-01 0 0
CUI: C1266176
Disease: Atypical choroid plexus papilloma
Atypical choroid plexus papilloma 		1 0 1 1.0E-01 0 0
CUI: C1280768
Disease: Axenfeld syndrome
Axenfeld syndrome 		1 0 1 1.0E-01 0 0
CUI: C1333100
Disease: Squamous cell carcinoma of colon
Squamous cell carcinoma of colon 		1 0 1 1.0E-01 0 0
CUI: C1843512
Disease: BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE 		1 0 1 1.0E-01 0 0
CUI: C1845108
Disease: Prominent median palatal raphe
Prominent median palatal raphe 		1 0 1 1.0E-01 0 0
CUI: C1858535
Disease: MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder)
MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1867327
Disease: RETINAL ARTERIES, TORTUOSITY OF
RETINAL ARTERIES, TORTUOSITY OF 		1 0 1 1.0E-01 0 0
CUI: C1968843
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C2675650
Disease: Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly 		1 0 1 1.0E-01 0 0
CUI: C2930808
Disease: Familial vascular leukoencephalopathy
Familial vascular leukoencephalopathy 		1 0 1 1.0E-01 0 0