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 1.4E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.5E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 1.5E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.5E-02
CUI: C0587178
Disease: Anti-nuclear antibody measurement
Anti-nuclear antibody measurement 		0 3 0 0 1 1.5E-02
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder 		0 3 0 0 2 3.0E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.5E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.5E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.5E-02
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 8.0E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 8.1E-04 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 0 1 8.1E-04 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 8.2E-04 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges 		52 0 1 8.2E-04 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 8.2E-04 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 1 8.2E-04 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 8.2E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 8.2E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 8.2E-04 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 8.2E-04 0 0
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		42 0 1 8.3E-04 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 8.3E-04 0 0
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		41 0 1 8.3E-04 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 1 8.3E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 8.3E-04 0 0