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: C0016202
Disease: Flatfoot
Flatfoot 		285 0 1 2.7E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.8E-03 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		276 0 1 2.8E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.8E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.9E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 3.0E-03 0 0
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 1 3.2E-03 0 0
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		843 0 3 3.3E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 3.3E-03 0 0
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders 		218 0 1 3.3E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 3.4E-03 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 0 1 3.4E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.5E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 3.5E-03 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		198 0 1 3.6E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		477 0 2 3.6E-03 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 0 1 3.6E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 3.7E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 3.7E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 3.7E-03 0 0
CUI: C1858085
Disease: Malar flattening
Malar flattening 		190 0 1 3.7E-03 0 0
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		187 0 1 3.7E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 3.7E-03 0 0
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
MAJOR AFFECTIVE DISORDER 2 		185 0 1 3.8E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 1 3.8E-03 0 0