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: C1852372
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder) 		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 7.1E-02
CUI: C0423122
Disease: Ptosis of eyebrow
Ptosis of eyebrow 		1 0 1 1.0E-01 0 0
CUI: C2751493
Disease: Cerebral Amyloid Angiopathy, Gsn-Related
Cerebral Amyloid Angiopathy, Gsn-Related 		1 0 1 1.0E-01 0 0
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: 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: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 1 9.1E-02 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis 		2 0 1 9.1E-02 0 0
CUI: C1864002
Disease: GRACILE SYNDROME (disorder)
GRACILE SYNDROME (disorder) 		2 27 1 9.1E-02 1 3.6E-02
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: C1622345
Disease: Meretoja syndrome
Meretoja syndrome 		3 0 1 8.3E-02 0 0
CUI: C4024863
Disease: Diffuse skin atrophy
Diffuse skin atrophy 		3 0 1 8.3E-02 0 0
CUI: C4025812
Disease: Dermatological manifestations of systemic disorders
Dermatological manifestations of systemic disorders 		3 0 1 8.3E-02 0 0
CUI: C4476761
Disease: Abnormal spleen morphology
Abnormal spleen morphology 		3 0 1 8.3E-02 0 0
CUI: C0005742
Disease: Blepharochalasis
Blepharochalasis 		4 0 1 7.7E-02 0 0
CUI: C0231689
Disease: Gait, Athetotic
Gait, Athetotic 		4 0 1 7.7E-02 0 0