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: C0220870
Disease: Lightheadedness
Lightheadedness 		1 0 1 4.8E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 4.8E-02 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 4.8E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 4.8E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 4.8E-02 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 4.8E-02 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 4.8E-02 0 0
CUI: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 4.8E-02 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 4.8E-02 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 4.8E-02 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 4.8E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 4.8E-02 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 4.8E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 4.8E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 4.8E-02 0 0
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		1 0 1 4.8E-02 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 4.8E-02 0 0
CUI: C1853202
Disease: PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO 		1 0 1 4.8E-02 0 0
CUI: C1854182
Disease: PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) 		1 0 1 4.8E-02 0 0
CUI: C1856476
Disease: Gaucher Disease, Type Iiic
Gaucher Disease, Type Iiic 		1 0 1 4.8E-02 0 0
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 4.8E-02 0 0
CUI: C1857747
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder) 		1 0 1 4.8E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 4.8E-02 0 0
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 0 1 4.8E-02 0 0
CUI: C1968942
Disease: Abnormal sacral segmentation
Abnormal sacral segmentation 		1 0 1 4.8E-02 0 0