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: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 3.1E-03
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 3.1E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 3.1E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 6.3E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 3.1E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.1E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 3.1E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 3.1E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.1E-03
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 6.2E-04 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 69 1 6.2E-04 1 2.6E-03
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis 		50 0 1 6.2E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 6.2E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 6.3E-04 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 6.3E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 6.3E-04 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 1 6.3E-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 6.3E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 6.3E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 6.3E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 6.3E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 6.3E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 6.3E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 6.3E-04 0 0