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: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 1.7E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 0 1 1.7E-03 0 0
CUI: C0018564
Disease: Hand deformities
Hand deformities 		60 0 1 1.7E-03 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 1 1.7E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.7E-03 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 1.7E-03 0 0
CUI: C0575157
Disease: Deformity of spine
Deformity of spine 		58 0 1 1.7E-03 0 0
CUI: C0005910
Disease: Body Weight
Body Weight 		57 0 1 1.7E-03 0 0
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 1.7E-03 0 0
CUI: C0424166
Disease: Social Anxiety
Social Anxiety 		57 0 1 1.7E-03 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		57 0 1 1.7E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		57 0 1 1.7E-03 0 0
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		57 0 1 1.7E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 1 1.7E-03 0 0
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		56 0 1 1.7E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 1.7E-03 0 0
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic 		55 0 1 1.7E-03 0 0
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		55 0 1 1.7E-03 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 1.7E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 1.7E-03 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 1.7E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 1.7E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		51 0 1 1.7E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 1.7E-03 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 1 1.7E-03 0 0