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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 1.5E-03
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 1.5E-03
CUI: C0523550
Disease: Catalase measurement
Catalase measurement 		0 2 0 0 1 1.5E-03
CUI: C1281440
Disease: Familial obesity
Familial obesity 		0 3 0 0 1 1.5E-03
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity 		0 3 0 0 1 1.5E-03
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.0E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 2.0E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 2.1E-03 0 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses 		194 0 1 2.1E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 2.1E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.1E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.2E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.2E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.2E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 2.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.2E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.2E-03 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 1 2.3E-03 0 0
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		149 527 1 2.3E-03 1 8.3E-04
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 2.3E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		147 526 1 2.3E-03 1 8.3E-04
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 526 1 2.3E-03 1 8.3E-04
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		147 526 1 2.3E-03 1 8.3E-04
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 2.3E-03 0 0