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: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 8 0.67 0 0
CUI: C3541471
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1 		2 13 2 0.20 1 7.7E-02
CUI: C3554605
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		1 0 1 1.0E-01 0 0
CUI: C3554606
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3 		1 0 1 1.0E-01 0 0
CUI: C3554607
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4 		1 0 1 1.0E-01 0 0
CUI: C3554608
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5 		1 0 1 1.0E-01 0 0
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		1 0 1 1.0E-01 0 0
CUI: C4014408
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 		1 0 1 1.0E-01 0 0
CUI: C4014440
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 		1 0 1 1.0E-01 0 0
CUI: C4016600
Disease: PARKINSONISM/MELAS OVERLAP SYNDROME
PARKINSONISM/MELAS OVERLAP SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C4016851
Disease: BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY 		1 0 1 1.0E-01 0 0
CUI: C4025631
Disease: Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes 		1 0 1 1.0E-01 0 0
CUI: C0272220
Disease: Chronic granulomatous disease, type II
Chronic granulomatous disease, type II 		2 0 1 9.1E-02 0 0
CUI: C0919785
Disease: Decreased transferrin saturation
Decreased transferrin saturation 		2 0 1 9.1E-02 0 0
CUI: C1864002
Disease: GRACILE SYNDROME (disorder)
GRACILE SYNDROME (disorder) 		2 0 1 9.1E-02 0 0
CUI: C4015253
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9 		2 0 1 9.1E-02 0 0
CUI: C4025022
Disease: Decreased mitochondrial complex III activity in liver tissue
Decreased mitochondrial complex III activity in liver tissue 		2 0 1 9.1E-02 0 0
CUI: C0231689
Disease: Gait, Athetotic
Gait, Athetotic 		4 0 1 7.7E-02 0 0
CUI: C0231693
Disease: Charcot Gait
Charcot Gait 		4 0 1 7.7E-02 0 0
CUI: C0231694
Disease: Gait, Festinating
Gait, Festinating 		4 0 1 7.7E-02 0 0
CUI: C0231695
Disease: Cerebellar ataxic gait
Cerebellar ataxic gait 		4 0 1 7.7E-02 0 0
CUI: C0231696
Disease: Gait, Hemiplegic
Gait, Hemiplegic 		4 0 1 7.7E-02 0 0
CUI: C0234996
Disease: Gait, Rigid
Gait, Rigid 		4 0 1 7.7E-02 0 0
CUI: C0235000
Disease: Gait, Broadened
Gait, Broadened 		4 0 1 7.7E-02 0 0
CUI: C0337210
Disease: Gait, Stumbling
Gait, Stumbling 		4 0 1 7.7E-02 0 0