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: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 2.9E-02 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 2.9E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 2.9E-02 0 0
CUI: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 2.9E-02 0 0
CUI: C2751320
Disease: Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay 		1 0 1 2.9E-02 0 0
CUI: C2919758
Disease: Deficiency of succinate-CoA ligase
Deficiency of succinate-CoA ligase 		1 0 1 2.9E-02 0 0
CUI: C3149750
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) 		1 0 1 2.9E-02 0 0
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		1 0 1 2.9E-02 0 0
CUI: C3151513
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) 		1 0 1 2.9E-02 0 0
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		1 0 1 2.9E-02 0 0
CUI: C3280378
Disease: MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA 		1 0 1 2.9E-02 0 0
CUI: C3501372
Disease: Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive
Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive 		1 0 1 2.9E-02 0 0
CUI: C3501891
Disease: Mitochondrial DNA Depletion Syndrome, Myopathic Form
Mitochondrial DNA Depletion Syndrome, Myopathic Form 		1 0 1 2.9E-02 0 0
CUI: C3554182
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15 		1 0 1 2.9E-02 0 0
CUI: C4013993
Disease: Bilateral striatal necrosis
Bilateral striatal necrosis 		1 0 1 2.9E-02 0 0
CUI: C4021521
Disease: Depletion of mitochondrial DNA in muscle tissue
Depletion of mitochondrial DNA in muscle tissue 		1 0 1 2.9E-02 0 0
CUI: C4025018
Disease: Depletion of mitochondrial DNA in liver
Depletion of mitochondrial DNA in liver 		1 0 1 2.9E-02 0 0
CUI: C4025595
Disease: Viral infection-induced rhabdomyolysis
Viral infection-induced rhabdomyolysis 		1 0 1 2.9E-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 2.9E-02 0 0
CUI: C4225391
Disease: MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY
MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY 		1 0 1 2.9E-02 0 0
CUI: C4304840
Disease: Progressive cavitating leukoencephalopathy
Progressive cavitating leukoencephalopathy 		1 0 1 2.9E-02 0 0
CUI: C4310733
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4 		1 0 1 2.9E-02 0 0
CUI: C4310734
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3 		1 0 1 2.9E-02 0 0
CUI: C4310935
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 		1 0 1 2.9E-02 0 0
CUI: C4318382
Disease: Cardiac Conduction Defects
Cardiac Conduction Defects 		1 0 1 2.9E-02 0 0