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: C0266484
Disease: Schizencephaly
Schizencephaly 		10 0 4 0.40 0 0
CUI: C1840529
Disease: HOLOPROSENCEPHALY 3
HOLOPROSENCEPHALY 3 		4 0 2 0.33 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 0.25 0 0
CUI: C0599949
Disease: Arterial Stiffness
Arterial Stiffness 		1 0 1 0.25 0 0
CUI: C0685869
Disease: Monophthalmos
Monophthalmos 		6 0 2 0.25 0 0
CUI: C1280768
Disease: Axenfeld syndrome
Axenfeld syndrome 		1 0 1 0.25 0 0
CUI: C1843512
Disease: BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE 		1 0 1 0.25 0 0
CUI: C1845108
Disease: Prominent median palatal raphe
Prominent median palatal raphe 		1 0 1 0.25 0 0
CUI: C1867327
Disease: RETINAL ARTERIES, TORTUOSITY OF
RETINAL ARTERIES, TORTUOSITY OF 		1 0 1 0.25 0 0
CUI: C1968843
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder) 		1 0 1 0.25 0 0
CUI: C2675650
Disease: Brain Small Vessel Disease With Axenfeld-Rieger Anomaly
Brain Small Vessel Disease With Axenfeld-Rieger Anomaly 		1 0 1 0.25 0 0
CUI: C2930808
Disease: Familial vascular leukoencephalopathy
Familial vascular leukoencephalopathy 		1 0 1 0.25 0 0
CUI: C3839990
Disease: Congenital stenosis of nasal pyriform aperture
Congenital stenosis of nasal pyriform aperture 		1 0 1 0.25 0 0
CUI: C4013035
Disease: BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES
BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES 		1 0 1 0.25 0 0
CUI: C0221011
Disease: Malignant Atrophic Papulosis
Malignant Atrophic Papulosis 		2 0 1 0.20 0 0
CUI: C0265581
Disease: Longitudinal deficiency of radius
Longitudinal deficiency of radius 		2 0 1 0.20 0 0
CUI: C0265740
Disease: Arrhinia
Arrhinia 		2 0 1 0.20 0 0
CUI: C0266981
Disease: Torus palatinus
Torus palatinus 		2 0 1 0.20 0 0
CUI: C0270173
Disease: TORCH syndrome
TORCH syndrome 		2 0 1 0.20 0 0
CUI: C0392550
Disease: Hemiplegia, Infantile
Hemiplegia, Infantile 		2 0 1 0.20 0 0
CUI: C1263853
Disease: Paralytic stroke
Paralytic stroke 		2 0 1 0.20 0 0
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		2 0 1 0.20 0 0
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 1 0.20 0 0
CUI: C1867983
Disease: PORENCEPHALY, FAMILIAL
PORENCEPHALY, FAMILIAL 		2 0 1 0.20 0 0
CUI: C3276742
Disease: Fibular duplication
Fibular duplication 		2 0 1 0.20 0 0