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: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.3E-02
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 4.2E-02
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 4.2E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 8.3E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 3.8E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 4.0E-02
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 4.0E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 2 1.7E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 1.8E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 2.0E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.0E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 2.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.0E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		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: C1836047
Disease: Long face
Long face 		182 0 1 2.1E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.1E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 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: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.2E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		160 0 1 2.2E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 1 2.2E-03 1 3.7E-03
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 2.2E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.2E-03 0 0