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: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 3 0.75 0 0
CUI: C0152516
Disease: Bacterial enteritis
Bacterial enteritis 		1 0 1 0.33 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 0.33 1 5.0E-02
CUI: C0275553
Disease: Bacterial cholangitis
Bacterial cholangitis 		1 0 1 0.33 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.33 0 0
CUI: C1865616
Disease: HEMOCHROMATOSIS, TYPE 2B
HEMOCHROMATOSIS, TYPE 2B 		1 0 1 0.33 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 0.33 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 0.33 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 0.33 1 4.8E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 0.33 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.33 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 0.33 1 4.8E-02
CUI: C3489571
Disease: Familial Extrahepatic Biliary Atresia
Familial Extrahepatic Biliary Atresia 		1 0 1 0.33 0 0
CUI: C3489572
Disease: Idiopathic Extrahepatic Biliary Atresia
Idiopathic Extrahepatic Biliary Atresia 		1 0 1 0.33 0 0
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 3 0.30 0 0
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		6 0 2 0.29 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 0.25 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 0.25 1 4.0E-02
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.25 0 0
CUI: C0398561
Disease: Glucose phosphate isomerase deficiency
Glucose phosphate isomerase deficiency 		2 0 1 0.25 0 0
CUI: C0740989
Disease: Chronic iron deficiency anaemia
Chronic iron deficiency anaemia 		2 0 1 0.25 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 0.25 0 0
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 0 1 0.25 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 0.25 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 0.25 0 0