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: C0235146
Disease: Euphoric mood
Euphoric mood 		1 0 1 4.3E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 4.3E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 4.3E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 4.3E-02 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 4.3E-02 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 4.3E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 4.3E-02 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 4.3E-02 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 4.3E-02 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 4.3E-02 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 4.3E-02 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 4.3E-02 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 4.3E-02 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 4.3E-02 0 0
CUI: C1836076
Disease: Amyotrophic Lateral Sclerosis, Chmp2B-Related
Amyotrophic Lateral Sclerosis, Chmp2B-Related 		1 0 1 4.3E-02 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 4.3E-02 0 0
CUI: C1837149
Disease: Alzheimer Disease 9
Alzheimer Disease 9 		1 0 1 4.3E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 4.3E-02 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 4.3E-02 0 0
CUI: C1843014
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques 		1 0 1 4.3E-02 0 0
CUI: C1843015
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia 		1 0 1 4.3E-02 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 4.3E-02 0 0
CUI: C1860219
Disease: Self-mutilation of tongue and lips due to involuntary movements
Self-mutilation of tongue and lips due to involuntary movements 		1 0 1 4.3E-02 0 0
CUI: C2677565
Disease: AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder) 		1 0 1 4.3E-02 0 0
CUI: C2732311
Disease: Multiple system atrophy, cerebellar variant
Multiple system atrophy, cerebellar variant 		1 0 1 4.3E-02 0 0