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: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 3 1.8E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 7.0E-03
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement 		0 51 0 0 50 0.35
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		96 0 1 1.1E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 1.1E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 1.1E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.1E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 1.1E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 1.1E-03 0 0
CUI: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow 		73 0 1 1.1E-03 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		71 0 1 1.1E-03 0 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		68 0 1 1.1E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.1E-03 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		65 0 1 1.1E-03 0 0
CUI: C0424448
Disease: Mask-like facies
Mask-like facies 		64 0 1 1.1E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 1.2E-03 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 1.2E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.2E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		57 0 1 1.2E-03 0 0
CUI: C1866730
Disease: Rhizomelia
Rhizomelia 		57 0 1 1.2E-03 0 0
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		55 0 1 1.2E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.2E-03 0 0
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		53 0 1 1.2E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 1.2E-03 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 1.2E-03 0 0