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: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 0 1 1.3E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 1.3E-03 0 0
CUI: C0023980
Disease: Longevity
Longevity 		48 0 1 1.3E-03 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 1.3E-03 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 1.3E-03 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 1.3E-03 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 1.3E-03 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 1.3E-03 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 1 1.3E-03 0 0
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		42 0 1 1.4E-03 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb 		42 0 1 1.4E-03 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 1 1.4E-03 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 1.4E-03 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 1.4E-03 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 1 1.4E-03 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology 		41 0 1 1.4E-03 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		40 0 1 1.4E-03 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		39 0 1 1.4E-03 0 0
CUI: C0234518
Disease: Slurred speech
Slurred speech 		39 0 1 1.4E-03 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly 		39 0 1 1.4E-03 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 1.4E-03 0 0
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		39 0 1 1.4E-03 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 1.4E-03 0 0
CUI: C0239399
Disease: Short extremities
Short extremities 		38 0 1 1.4E-03 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 1 1.4E-03 0 0