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: C0392185
Disease: Verbal repetition
Verbal repetition 		3 0 2 0.33 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 2 0.33 0 0
CUI: C4021076
Disease: Iron accumulation in brain
Iron accumulation in brain 		3 0 2 0.33 0 0
CUI: C4510873
Disease: Atypical juvenile parkinsonism
Atypical juvenile parkinsonism 		4 0 2 0.29 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 3 0.27 0 0
CUI: C4024929
Disease: Slowed slurred speech
Slowed slurred speech 		5 0 2 0.25 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 0.20 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 0.20 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 0.20 0 0
CUI: C0393577
Disease: Pallidal degeneration
Pallidal degeneration 		1 0 1 0.20 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 0.20 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 0.20 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 0.20 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy 		19 0 4 0.20 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 0.20 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 0.20 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 0.20 0 0
CUI: C1857747
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder) 		1 0 1 0.20 0 0
CUI: C2750220
Disease: Karak Syndrome
Karak Syndrome 		1 0 1 0.20 0 0
CUI: C2751506
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL 		1 0 1 0.20 0 0
CUI: C3809824
Disease: PARKINSON DISEASE 20, EARLY-ONSET
PARKINSON DISEASE 20, EARLY-ONSET 		1 0 1 0.20 0 0
CUI: C4022743
Disease: T2 hypointense basal ganglia
T2 hypointense basal ganglia 		1 0 1 0.20 0 0
CUI: C4022768
Disease: Cerebellar gliosis
Cerebellar gliosis 		1 0 1 0.20 0 0
CUI: C4024962
Disease: Axial muscle stiffness
Axial muscle stiffness 		1 0 1 0.20 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.20 0 0