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: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 		1 0 1 0.11 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 0.11 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 0.11 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 0.11 0 0
CUI: C2751427
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO 		1 0 1 0.11 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 0.11 0 0
CUI: C3275684
Disease: MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1 		1 0 1 0.11 0 0
CUI: C3539120
Disease: PROSTATE CANCER, HEREDITARY, 2
PROSTATE CANCER, HEREDITARY, 2 		1 0 1 0.11 0 0
CUI: C3665332
Disease: Primary hypertrophic cardiomyopathy
Primary hypertrophic cardiomyopathy 		1 0 1 0.11 0 0
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		1 0 1 0.11 0 0
CUI: C3809346
Disease: CARDIOMYOPATHY, DILATED, 1MM
CARDIOMYOPATHY, DILATED, 1MM 		1 0 1 0.11 0 0
CUI: C3809526
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17 		1 0 1 0.11 0 0
CUI: C4016603
Disease: SEIZURES AND LACTIC ACIDOSIS
SEIZURES AND LACTIC ACIDOSIS 		1 0 1 0.11 0 0
CUI: C4225415
Disease: MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3
MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3 		1 0 1 0.11 0 0
CUI: C4748769
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11 		1 0 1 0.11 0 0
CUI: C4755299
Disease: MT-ATP6-related mitochondrial spastic paraplegia
MT-ATP6-related mitochondrial spastic paraplegia 		1 0 1 0.11 0 0
CUI: C1963282
Disease: Wolff-Parkinson-White Syndrome, CTCAE
Wolff-Parkinson-White Syndrome, CTCAE 		2 0 1 1.0E-01 0 0
CUI: C3275686
Disease: CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY
CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY 		2 0 2 0.22 0 0
CUI: C3554534
Disease: CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2 		2 2 1 1.0E-01 1 0.25
CUI: C4016621
Disease: Mitochondrial neurogastrointestinal encephalomyopathy syndrome
Mitochondrial neurogastrointestinal encephalomyopathy syndrome 		2 0 1 1.0E-01 0 0
CUI: C4751573
Disease: Periodic paralysis with later-onset distal motor neuropathy
Periodic paralysis with later-onset distal motor neuropathy 		2 0 2 0.22 0 0
CUI: C0026755
Disease: Multiple Carboxylase Deficiency
Multiple Carboxylase Deficiency 		3 0 1 9.1E-02 0 0
CUI: C0232310
Disease: P mitrale (finding)
P mitrale (finding) 		3 0 1 9.1E-02 0 0
CUI: C0238705
Disease: Left atrial hypertrophy
Left atrial hypertrophy 		3 0 1 9.1E-02 0 0
CUI: C1837148
Disease: MYOPIA 6 (disorder)
MYOPIA 6 (disorder) 		3 0 1 9.1E-02 0 0