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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.7E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 3.7E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.7E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 3.7E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.7E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.7E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.7E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.7E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.7E-03
CUI: C0231687
Disease: Spastic gait
Spastic gait 		62 0 1 7.6E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 7.6E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 7.6E-04 0 0
CUI: C0455988
Disease: Hydrops Fetalis, Non-Immune
Hydrops Fetalis, Non-Immune 		51 0 1 7.7E-04 0 0
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 0 1 7.7E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 7.7E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 7.7E-04 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 7.7E-04 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 1 7.7E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 7.7E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 7.7E-04 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 1 7.7E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 69 1 7.7E-04 1 3.0E-03
CUI: C0858600
Disease: Taste sweet
Taste sweet 		41 0 1 7.7E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 7.7E-04 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 1 7.7E-04 0 0