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: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 1.2E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 1.2E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.2E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 1.2E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.2E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 1.2E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 1.2E-03 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 1 1.2E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 1.2E-03 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 1.2E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.2E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 1.2E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 1.2E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.2E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 1.2E-03 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag 		53 0 1 1.2E-03 0 0
CUI: C0455988
Disease: Hydrops Fetalis, Non-Immune
Hydrops Fetalis, Non-Immune 		51 0 1 1.2E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 1.2E-03 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 1 1.2E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.2E-03 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 1 1.2E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 1.2E-03 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 1.2E-03 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 1 1.2E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.2E-03 0 0