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: C0422837
Disease: Neurological observations
Neurological observations 		6 0 6 0.46 0 0
CUI: C0746857
Disease: Focal Neurologic Deficits
Focal Neurologic Deficits 		6 0 6 0.46 0 0
CUI: C0751377
Disease: Neurologic Dysfunction
Neurologic Dysfunction 		6 0 6 0.46 0 0
CUI: C0521654
Disease: Neurologic Deficits
Neurologic Deficits 		8 0 6 0.40 0 0
CUI: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		12 0 6 0.32 0 0
CUI: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia 		9 0 2 1.0E-01 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 7.7E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 7.7E-02 0 0
CUI: C0221027
Disease: Immunodeficiency with thymoma
Immunodeficiency with thymoma 		1 0 1 7.7E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 7.7E-02 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia 		15 0 2 7.7E-02 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 7.7E-02 0 0
CUI: C1274923
Disease: Cutaneous hyperalgesia
Cutaneous hyperalgesia 		1 0 1 7.7E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 7.7E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 7.7E-02 0 0
CUI: C1834569
Disease: Jankovic Rivera syndrome
Jankovic Rivera syndrome 		1 0 1 7.7E-02 0 0
CUI: C1856476
Disease: Gaucher Disease, Type Iiic
Gaucher Disease, Type Iiic 		1 19 1 7.7E-02 1 5.3E-02
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 7.7E-02 0 0
CUI: C1864567
Disease: CATARACT, POSTERIOR POLAR, 4 (disorder)
CATARACT, POSTERIOR POLAR, 4 (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1970386
Disease: Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities
Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities 		1 0 1 7.7E-02 0 0
CUI: C2676021
Disease: DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO
DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO 		1 0 1 7.7E-02 0 0
CUI: C2931585
Disease: Gaucher-like disease
Gaucher-like disease 		1 0 1 7.7E-02 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 7.7E-02 0 0
CUI: C3495555
Disease: Carnosinemia
Carnosinemia 		1 0 1 7.7E-02 0 0
CUI: C3807150
Disease: CATARACT 11, POSTERIOR POLAR
CATARACT 11, POSTERIOR POLAR 		1 0 1 7.7E-02 0 0