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: C0393560
Disease: Vascular Dementia, Acute Onset
Vascular Dementia, Acute Onset 		1 0 1 1.00 0 0
CUI: C0270786
Disease: Binswanger Disease
Binswanger Disease 		4 0 1 0.25 0 0
CUI: C4025278
Disease: Stress/infection-induced lactic acidosis
Stress/infection-induced lactic acidosis 		4 0 1 0.25 0 0
CUI: C4476644
Disease: Segmental myoclonic seizures
Segmental myoclonic seizures 		5 0 1 0.20 0 0
CUI: C1855010
Disease: Progressive leukoencephalopathy
Progressive leukoencephalopathy 		7 0 1 0.14 0 0
CUI: C4024705
Disease: Decreased activity of mitochondrial complex II
Decreased activity of mitochondrial complex II 		7 0 1 0.14 0 0
CUI: C4025244
Disease: Abnormal atrioventricular conduction
Abnormal atrioventricular conduction 		7 0 1 0.14 0 0
CUI: C0342777
Disease: Succinate-coenzyme Q reductase deficiency
Succinate-coenzyme Q reductase deficiency 		8 0 1 0.12 0 0
CUI: C0393561
Disease: Subcortical Vascular Dementia
Subcortical Vascular Dementia 		8 0 1 0.12 0 0
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency 		8 0 1 0.12 0 0
CUI: C1856565
Disease: Progressive psychomotor deterioration
Progressive psychomotor deterioration 		11 0 1 9.1E-02 0 0
CUI: C1836806
Disease: Mild microcephaly
Mild microcephaly 		12 0 1 8.3E-02 0 0
CUI: C0240116
Disease: Hyperactive patellar reflex
Hyperactive patellar reflex 		14 0 1 7.1E-02 0 0
CUI: C1866284
Disease: Motor deterioration
Motor deterioration 		14 0 1 7.1E-02 0 0
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs 		16 0 1 6.2E-02 0 0
CUI: C1839832
Disease: Noncompaction cardiomyopathy
Noncompaction cardiomyopathy 		17 0 1 5.9E-02 0 0
CUI: C1845245
Disease: Lower limb hypertonia
Lower limb hypertonia 		21 0 1 4.8E-02 0 0
CUI: C2237142
Disease: Moderate global developmental delay
Moderate global developmental delay 		27 0 1 3.7E-02 0 0
CUI: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		27 0 1 3.7E-02 0 0
CUI: C1533847
Disease: Disorder of skeletal muscle
Disorder of skeletal muscle 		29 0 1 3.4E-02 0 0
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		30 0 1 3.3E-02 0 0
CUI: C1846176
Disease: Hyperactive deep tendon reflexes
Hyperactive deep tendon reflexes 		32 0 1 3.1E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 1 2.9E-02 0 0
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk 		37 0 1 2.7E-02 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 2.6E-02 0 0