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: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 7.7E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 7.7E-02 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 7.7E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 1 1 7.7E-02 1 0.25
CUI: C1857747
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder) 		1 0 1 7.7E-02 0 0
CUI: C2750220
Disease: Karak Syndrome
Karak Syndrome 		1 0 1 7.7E-02 0 0
CUI: C2938912
Disease: Hyperintensity of cerebral white matter on MRI
Hyperintensity of cerebral white matter on MRI 		15 0 2 7.7E-02 0 0
CUI: C3553816
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13 		1 0 1 7.7E-02 0 0
CUI: C4020920
Disease: Enlarged interhemispheric fissure
Enlarged interhemispheric fissure 		1 0 1 7.7E-02 0 0
CUI: C4022743
Disease: T2 hypointense basal ganglia
T2 hypointense basal ganglia 		1 0 1 7.7E-02 0 0
CUI: C4022768
Disease: Cerebellar gliosis
Cerebellar gliosis 		1 0 1 7.7E-02 0 0
CUI: C4023074
Disease: EEG with parietal focal spikes
EEG with parietal focal spikes 		1 1 1 7.7E-02 1 0.25
CUI: C4023405
Disease: Abnormality of ocular abduction
Abnormality of ocular abduction 		1 0 1 7.7E-02 0 0
CUI: C4024962
Disease: Axial muscle stiffness
Axial muscle stiffness 		1 0 1 7.7E-02 0 0
CUI: C4225205
Disease: SPINOCEREBELLAR ATAXIA 42
SPINOCEREBELLAR ATAXIA 42 		1 0 1 7.7E-02 0 0
CUI: C4280687
Disease: Upper limb muscle hypertrophy
Upper limb muscle hypertrophy 		1 0 1 7.7E-02 0 0
CUI: C4310633
Disease: DYSTONIA 28, CHILDHOOD-ONSET
DYSTONIA 28, CHILDHOOD-ONSET 		1 17 1 7.7E-02 1 5.0E-02
CUI: C4310763
Disease: SPINOCEREBELLAR ATAXIA 43
SPINOCEREBELLAR ATAXIA 43 		1 0 1 7.7E-02 0 0
CUI: C4324277
Disease: Myokymia of eyelid
Myokymia of eyelid 		1 0 1 7.7E-02 0 0
CUI: C4479653
Disease: SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY
SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY 		1 0 1 7.7E-02 0 0
CUI: C4732764
Disease: Tachylalia
Tachylalia 		1 0 1 7.7E-02 0 0
CUI: C4748120
Disease: SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS
SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS 		1 0 1 7.7E-02 0 0
CUI: C4748934
Disease: NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY
NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY 		1 8 1 7.7E-02 2 0.20
CUI: C0038661
Disease: Suicide
Suicide 		2 0 1 7.1E-02 0 0
CUI: C0454582
Disease: Semantic impairment
Semantic impairment 		2 0 1 7.1E-02 0 0