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: C0042834
Disease: Vital capacity
Vital capacity 		430 0 1 1.8E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 1 1.9E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 0 1 2.2E-03 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		681 0 2 2.5E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 0 1 2.5E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		269 0 1 2.5E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.6E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		265 0 1 2.6E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.6E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 2.7E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		234 0 1 2.8E-03 0 0
CUI: C0007129
Disease: Merkel cell carcinoma
Merkel cell carcinoma 		226 0 1 2.9E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.9E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.9E-03 0 0
CUI: C0005612
Disease: Birth Weight
Birth Weight 		214 0 1 3.0E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 3.0E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 3.0E-03 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		210 0 1 3.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.0E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 3.0E-03 0 0
CUI: C1527349
Disease: Ductal Breast Carcinoma
Ductal Breast Carcinoma 		196 0 1 3.1E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 3.1E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 3.2E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 3.3E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.3E-03 0 0