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: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 5.6E-02 0 0
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL 		1 0 1 5.6E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 5.6E-02 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 5.6E-02 0 0
CUI: C1838954
Disease: STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA
STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA 		1 0 1 5.6E-02 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 5.6E-02 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 5.6E-02 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 5.6E-02 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 5.6E-02 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 5.6E-02 0 0
CUI: C4016603
Disease: SEIZURES AND LACTIC ACIDOSIS
SEIZURES AND LACTIC ACIDOSIS 		1 0 1 5.6E-02 0 0
CUI: C4016615
Disease: CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY
CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY 		1 0 1 5.6E-02 0 0
CUI: C4016616
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH 		1 0 1 5.6E-02 0 0
CUI: C4016618
Disease: NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT
NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT 		1 0 1 5.6E-02 0 0
CUI: C4016620
Disease: CARDIOMYOPATHY AND DEAFNESS
CARDIOMYOPATHY AND DEAFNESS 		1 0 1 5.6E-02 0 0
CUI: C4016622
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MYOCLONUS
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MYOCLONUS 		1 0 1 5.6E-02 0 0
CUI: C4016629
Disease: NEUROGASTROINTESTINAL SYNDROME, MITOCHONDRIAL
NEUROGASTROINTESTINAL SYNDROME, MITOCHONDRIAL 		1 0 1 5.6E-02 0 0
CUI: C4016630
Disease: ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL
ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL 		1 0 1 5.6E-02 0 0
CUI: C4016634
Disease: ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS 		1 0 1 5.6E-02 0 0
CUI: C4017627
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MATERNALLY TRANSMITTED
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MATERNALLY TRANSMITTED 		1 0 1 5.6E-02 0 0
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL 		1 0 1 5.6E-02 0 0
CUI: C4225246
Disease: SURF1-related Charcot-Marie-Tooth disease type 4
SURF1-related Charcot-Marie-Tooth disease type 4 		1 0 1 5.6E-02 0 0
CUI: C4225415
Disease: MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3
MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3 		1 0 1 5.6E-02 0 0
CUI: C4275073
Disease: Desmin related myopathy with Mallory body-like inclusions
Desmin related myopathy with Mallory body-like inclusions 		1 0 1 5.6E-02 0 0
CUI: C4722144
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3 (finding)
MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3 (finding) 		1 0 1 5.6E-02 0 0