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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 9.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.33
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0 61 0 0 1 1.6E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 8.0E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 0.33
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 0.20
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 0.25
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.33
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 0.20
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.33
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 0.25
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 0.50
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		523 0 1 1.7E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index 		1014 0 2 1.8E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia 		453 0 1 1.9E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 1 2.0E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 1 2.0E-03 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		393 0 1 2.1E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking 		391 0 1 2.1E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.2E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay 		384 0 1 2.2E-03 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		340 0 1 2.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 2.5E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 1 2.6E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		305 0 1 2.6E-03 0 0