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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 5.6E-02 0 0
CUI: C0033931
Disease: Psychophysiologic Disorders
Psychophysiologic Disorders 		1 0 1 5.6E-02 0 0
CUI: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal 		1 0 1 5.6E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 5.6E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 5.6E-02 0 0
CUI: C0338900
Disease: Psychasthenic neurosis
Psychasthenic neurosis 		1 0 1 5.6E-02 0 0
CUI: C0454601
Disease: Pyramidal dysarthria
Pyramidal dysarthria 		1 0 1 5.6E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 5.6E-02 0 0
CUI: C0542165
Disease: Pseudoparkinsonism
Pseudoparkinsonism 		1 0 1 5.6E-02 0 0
CUI: C0751668
Disease: Machado-Joseph Disease Type I
Machado-Joseph Disease Type I 		1 0 1 5.6E-02 0 0
CUI: C0751669
Disease: Machado-Joseph Disease Type II
Machado-Joseph Disease Type II 		1 0 1 5.6E-02 0 0
CUI: C0751670
Disease: Machado-Joseph Disease Type III
Machado-Joseph Disease Type III 		1 0 1 5.6E-02 0 0
CUI: C0751671
Disease: Machado-Joseph Disease Type IV
Machado-Joseph Disease Type IV 		1 0 1 5.6E-02 0 0
CUI: C0848200
Disease: Afterbirth pain
Afterbirth pain 		1 0 1 5.6E-02 0 0
CUI: C1389273
Disease: Lesions in the basal ganglia
Lesions in the basal ganglia 		1 0 1 5.6E-02 0 0
CUI: C1837154
Disease: Drug Metabolism, Poor, CYP2D6-Related
Drug Metabolism, Poor, CYP2D6-Related 		1 0 1 5.6E-02 0 0
CUI: C1838049
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 1
Epilepsy, Nocturnal Frontal Lobe, Type 1 		1 0 1 5.6E-02 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 5.6E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 0 1 5.6E-02 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 5.6E-02 0 0
CUI: C1862359
Disease: Facial-lingual fasciculations
Facial-lingual fasciculations 		1 0 1 5.6E-02 0 0
CUI: C1865818
Disease: DYSTONIA 7, TORSION (disorder)
DYSTONIA 7, TORSION (disorder) 		1 0 1 5.6E-02 0 0
CUI: C1865819
Disease: CERVICAL DYSTONIA, PRIMARY
CERVICAL DYSTONIA, PRIMARY 		1 0 1 5.6E-02 0 0
CUI: C2363747
Disease: Neurological decompensation
Neurological decompensation 		1 0 1 5.6E-02 0 0
CUI: C2937300
Disease: Congenital hereditary muscular dystrophy
Congenital hereditary muscular dystrophy 		1 0 1 5.6E-02 0 0