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: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 1 1.4E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 0 1 2.1E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 2.2E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.3E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 0 1 2.5E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		272 0 1 2.5E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.6E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.7E-03 0 0
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 0 1 2.8E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 2.9E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 3.0E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.0E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 3.0E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 3.1E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 3.1E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 3.1E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 3.2E-03 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		497 0 2 3.2E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 3.2E-03 0 0
CUI: C0239234
Disease: Low set ears
Low set ears 		489 0 2 3.2E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 3.2E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 3.2E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.3E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 3.3E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 3.3E-03 0 0