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: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 7.3E-04 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		57 0 1 7.3E-04 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		57 0 1 7.3E-04 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 7.4E-04 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 7.4E-04 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		51 0 1 7.4E-04 0 0
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		50 0 1 7.4E-04 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 7.4E-04 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux 		48 0 1 7.4E-04 0 0
CUI: C0086439
Disease: Hypokinesia
Hypokinesia 		47 0 1 7.4E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 7.4E-04 0 0
CUI: C1845447
Disease: Cupped ears (finding)
Cupped ears (finding) 		45 0 1 7.4E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 7.4E-04 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 7.4E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 7.4E-04 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 1 7.4E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 7.4E-04 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 1 7.4E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 7.4E-04 0 0
CUI: C4082169
Disease: Metatarsus Varus
Metatarsus Varus 		41 0 1 7.4E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 7.4E-04 0 0
CUI: C0266610
Disease: Preauricular dimple
Preauricular dimple 		40 0 1 7.4E-04 0 0
CUI: C1285654
Disease: Memory performance
Memory performance 		40 0 1 7.4E-04 0 0
CUI: C1398312
Disease: Narrow palate
Narrow palate 		40 0 1 7.4E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 7.4E-04 0 0