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: C0268090
Disease: Manganese deficiency
Manganese deficiency 		1 0 1 0.33 0 0
CUI: C4022419
Disease: Abnormal transferrin saturation
Abnormal transferrin saturation 		1 0 1 0.33 0 0
CUI: C4310765
Disease: Hypermanganesemia with dystonia 2
Hypermanganesemia with dystonia 2 		1 0 1 0.33 0 0
CUI: C0854060
Disease: Increased total iron binding capacity
Increased total iron binding capacity 		2 0 1 0.25 0 0
CUI: C1840404
Disease: Hyperostosis Cranialis Interna
Hyperostosis Cranialis Interna 		2 0 1 0.25 0 0
CUI: C2750442
Disease: Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		2 0 1 0.25 0 0
CUI: C3672035
Disease: Copper accumulation in liver
Copper accumulation in liver 		2 0 1 0.25 0 0
CUI: C4025022
Disease: Decreased mitochondrial complex III activity in liver tissue
Decreased mitochondrial complex III activity in liver tissue 		2 0 1 0.25 0 0
CUI: C0241012
Disease: Decreased serum ferritin
Decreased serum ferritin 		3 0 1 0.20 0 0
CUI: C1858725
Disease: NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1
NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1 		3 0 1 0.20 0 0
CUI: C4476760
Disease: Visual fixation instability
Visual fixation instability 		3 0 1 0.20 0 0
CUI: C0677050
Disease: Manganese Poisoning
Manganese Poisoning 		16 0 3 0.19 0 0
CUI: C1735368
Disease: Acute dystonia
Acute dystonia 		4 0 1 0.17 0 0
CUI: C4021624
Disease: Osteosclerosis of the base of the skull
Osteosclerosis of the base of the skull 		4 0 1 0.17 0 0
CUI: C1834737
Disease: Cutaneous syndactyly of toes
Cutaneous syndactyly of toes 		5 0 1 0.14 0 0
CUI: C1842836
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii 		6 0 1 0.12 0 0
CUI: C4020800
Disease: Decreased activity of mitochondrial complex IV
Decreased activity of mitochondrial complex IV 		6 0 1 0.12 0 0
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		7 0 1 0.11 0 0
CUI: C4021094
Disease: Type II transferrin isoform profile
Type II transferrin isoform profile 		7 0 1 0.11 0 0
CUI: C4022745
Disease: Abnormal basal ganglia MRI signal intensity
Abnormal basal ganglia MRI signal intensity 		7 0 1 0.11 0 0
CUI: C4024705
Disease: Decreased activity of mitochondrial complex II
Decreased activity of mitochondrial complex II 		7 0 1 0.11 0 0
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		8 0 1 1.0E-01 0 0
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism 		9 0 1 9.1E-02 0 0
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis 		9 0 1 9.1E-02 0 0
CUI: C2677590
Disease: Congenital Disorder Of Glycosylation, Type In
Congenital Disorder Of Glycosylation, Type In 		9 0 1 9.1E-02 0 0