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: C3554605
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		1 0 1 0.50 0 0
CUI: C4016851
Disease: BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY 		1 2 1 0.50 1 7.1E-02
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 0.50 0 0
CUI: C0919785
Disease: Decreased transferrin saturation
Decreased transferrin saturation 		2 0 1 0.33 0 0
CUI: C1864002
Disease: GRACILE SYNDROME (disorder)
GRACILE SYNDROME (disorder) 		2 27 1 0.33 3 8.1E-02
CUI: C4025022
Disease: Decreased mitochondrial complex III activity in liver tissue
Decreased mitochondrial complex III activity in liver tissue 		2 0 1 0.33 0 0
CUI: C0231689
Disease: Gait, Athetotic
Gait, Athetotic 		4 0 1 0.20 0 0
CUI: C0231693
Disease: Charcot Gait
Charcot Gait 		4 0 1 0.20 0 0
CUI: C0231694
Disease: Gait, Festinating
Gait, Festinating 		4 0 1 0.20 0 0
CUI: C0231695
Disease: Cerebellar ataxic gait
Cerebellar ataxic gait 		4 0 1 0.20 0 0
CUI: C0231696
Disease: Gait, Hemiplegic
Gait, Hemiplegic 		4 0 1 0.20 0 0
CUI: C0234996
Disease: Gait, Rigid
Gait, Rigid 		4 0 1 0.20 0 0
CUI: C0235000
Disease: Gait, Broadened
Gait, Broadened 		4 0 1 0.20 0 0
CUI: C0337210
Disease: Gait, Stumbling
Gait, Stumbling 		4 0 1 0.20 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 2 2 0.20 1 7.1E-02
CUI: C0427128
Disease: Rapid Fatigue of Gait
Rapid Fatigue of Gait 		4 0 1 0.20 0 0
CUI: C0427169
Disease: Marche a Petit Pas
Marche a Petit Pas 		4 0 1 0.20 0 0
CUI: C0427177
Disease: Gait, Hysterical
Gait, Hysterical 		4 0 1 0.20 0 0
CUI: C0751829
Disease: Gait Disorder, Sensorimotor
Gait Disorder, Sensorimotor 		4 0 1 0.20 0 0
CUI: C0751830
Disease: Gait Disorders, Neurologic
Gait Disorders, Neurologic 		4 0 1 0.20 0 0
CUI: C0751831
Disease: Gait, Frontal
Gait, Frontal 		4 0 1 0.20 0 0
CUI: C0751832
Disease: Gait, Widebased
Gait, Widebased 		4 0 1 0.20 0 0
CUI: C1839437
Disease: Chronic lactic acidosis
Chronic lactic acidosis 		4 0 1 0.20 0 0
CUI: C1852372
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder) 		10 1 2 0.20 1 7.7E-02
CUI: C0268344
Disease: Ehlers-Danlos syndrome 6B
Ehlers-Danlos syndrome 6B 		5 0 1 0.17 0 0