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: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 9 8.5E-02 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 9 8.5E-02 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait 		62 0 7 8.4E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 8 8.4E-02 0 0
CUI: C0151564
Disease: Cogwheel Rigidity
Cogwheel Rigidity 		24 0 4 8.3E-02 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder 		11 0 3 8.3E-02 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 3 8.1E-02 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 3 8.1E-02 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		102 0 9 7.4E-02 0 0
CUI: C3805715
Disease: Short stepped shuffling gait
Short stepped shuffling gait 		16 0 3 7.3E-02 0 0
CUI: C0751772
Disease: REM Sleep Behavior Disorder
REM Sleep Behavior Disorder 		46 0 5 7.2E-02 0 0
CUI: C1846176
Disease: Hyperactive deep tendon reflexes
Hyperactive deep tendon reflexes 		32 2 4 7.1E-02 1 0.33
CUI: C0085631
Disease: Agitation
Agitation 		109 0 9 7.0E-02 0 0
CUI: C0151583
Disease: Abnormality of the cerebrospinal fluid
Abnormality of the cerebrospinal fluid 		3 0 2 6.9E-02 0 0
CUI: C0155320
Disease: Blindness, Cortical
Blindness, Cortical 		3 0 2 6.9E-02 0 0
CUI: C1859520
Disease: Progressive spasticity
Progressive spasticity 		19 0 3 6.8E-02 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 5 6.8E-02 0 0
CUI: C0426980
Disease: Motor symptoms
Motor symptoms 		100 0 8 6.7E-02 0 0
CUI: C1850303
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 		4 0 2 6.7E-02 0 0
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology 		20 0 3 6.7E-02 0 0
CUI: C4510873
Disease: Atypical juvenile parkinsonism
Atypical juvenile parkinsonism 		4 0 2 6.7E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease 		37 0 4 6.6E-02 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive 		38 0 4 6.5E-02 0 0
CUI: C4024929
Disease: Slowed slurred speech
Slowed slurred speech 		5 0 2 6.5E-02 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 3 6.4E-02 0 0