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: C0750834
Disease: hyperthyroid cardiac disease
hyperthyroid cardiac disease 		1 0 1 0.50 0 0
CUI: C1275422
Disease: Relapsing linear acantholytic dermatosis
Relapsing linear acantholytic dermatosis 		1 0 1 0.50 0 0
CUI: C4022419
Disease: Abnormal transferrin saturation
Abnormal transferrin saturation 		1 0 1 0.50 0 0
CUI: C0854060
Disease: Increased total iron binding capacity
Increased total iron binding capacity 		2 0 1 0.33 0 0
CUI: C3672035
Disease: Copper accumulation in liver
Copper accumulation in liver 		2 0 1 0.33 0 0
CUI: C0241012
Disease: Decreased serum ferritin
Decreased serum ferritin 		3 0 1 0.25 0 0
CUI: C4225234
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn 		3 0 1 0.25 0 0
CUI: C4022745
Disease: Abnormal basal ganglia MRI signal intensity
Abnormal basal ganglia MRI signal intensity 		7 0 1 0.12 0 0
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		8 0 1 0.11 0 0
CUI: C0271791
Disease: Severe hypothyroidism
Severe hypothyroidism 		9 0 1 1.0E-01 0 0
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis 		9 0 1 1.0E-01 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology 		10 0 1 9.1E-02 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 8.3E-02 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 1 6.7E-02 0 0
CUI: C0677050
Disease: Manganese Poisoning
Manganese Poisoning 		16 0 1 5.9E-02 0 0
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism 		18 0 1 5.3E-02 0 0
CUI: C0267812
Disease: Micronodular cirrhosis
Micronodular cirrhosis 		18 0 1 5.3E-02 0 0
CUI: C0393610
Disease: Dystonia, Diurnal
Dystonia, Diurnal 		18 0 1 5.3E-02 0 0
CUI: C0752203
Disease: Dystonia, Primary
Dystonia, Primary 		19 0 1 5.0E-02 0 0
CUI: C4316995
Disease: Primary Hypothyroidism
Primary Hypothyroidism 		19 0 1 5.0E-02 0 0
CUI: C3814530
Disease: Skin Vesicle
Skin Vesicle 		20 0 1 4.8E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 1 3.4E-02 0 0
CUI: C0393588
Disease: Dystonia, Paroxysmal
Dystonia, Paroxysmal 		28 0 1 3.4E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 1 3.4E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 1 3.4E-02 0 0