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: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 1.6E-03 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 1.6E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 1.6E-03 0 0
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 0 1 1.6E-03 0 0
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		50 0 1 1.6E-03 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 1.6E-03 0 0
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		50 0 1 1.6E-03 0 0
CUI: C0233844
Disease: Clumsiness
Clumsiness 		48 0 1 1.6E-03 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 1 1.6E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.6E-03 0 0
CUI: C2673431
Disease: Abnormality of the periventricular white matter
Abnormality of the periventricular white matter 		45 0 1 1.6E-03 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies 		44 0 1 1.6E-03 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 1 1.6E-03 0 0
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		44 0 1 1.6E-03 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 1.6E-03 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 1.6E-03 0 0
CUI: C0426818
Disease: Thin rib
Thin rib 		42 0 1 1.6E-03 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb 		42 0 1 1.6E-03 0 0
CUI: C0751093
Disease: Dystonia, Limb
Dystonia, Limb 		42 0 1 1.6E-03 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 1 1.6E-03 0 0
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		41 0 1 1.6E-03 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 1 1.6E-03 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity 		41 0 1 1.6E-03 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 1 1.6E-03 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 1.6E-03 0 0