Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Encephalopathy, Subacute Necrotizing, Infantile
9 0 1 0.11 0 0
Encephalopathy, Subacute Necrotizing, Juvenile
9 0 1 0.11 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 3.0E-02 0 0
Decreased activity of mitochondrial respiratory chain
34 0 1 2.9E-02 0 0
Decreased activity of the pyruvate dehydrogenase complex
35 0 1 2.9E-02 0 0
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
36 0 1 2.8E-02 0 0
Leigh Syndrome due to Mitochondrial Complex III Deficiency
36 0 1 2.8E-02 0 0
Leigh Syndrome due to Mitochondrial Complex V Deficiency
36 0 1 2.8E-02 0 0
Necrotizing encephalopathy, infantile subacute, of Leigh
36 0 1 2.8E-02 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 1 2.7E-02 0 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
37 0 1 2.7E-02 0 0
Paroxysmal involuntary eye movements
39 0 1 2.6E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 2.6E-02 0 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 2.5E-02 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 2.5E-02 0 0
Decreased activity of mitochondrial complex I
41 0 1 2.4E-02 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis
42 0 1 2.4E-02 0 0
CUI: C0015930
Disease: Fetal Distress
Fetal Distress
44 0 1 2.3E-02 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate
45 0 1 2.2E-02 0 0
Focal T2 hyperintense basal ganglia lesion
46 0 1 2.2E-02 0 0
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
51 0 1 2.0E-02 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia
59 0 1 1.7E-02 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 0 1 1.5E-02 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact
73 0 1 1.4E-02 0 0
Non-ST Elevated Myocardial Infarction
85 0 1 1.2E-02 0 0