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: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 1.00 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 1.00 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 1.00 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 1.00 1 0.50
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 1.00 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 1.00 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 1.00 1 0.50
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 0.50 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 0.50 1 0.17
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.50 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 0.50 0 0
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 0 1 0.50 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 0.50 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 0.50 0 0
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		3 0 1 0.33 0 0
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 20 1 0.33 1 5.0E-02
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 1 0.33 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 3 1 0.25 1 0.33
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 1 0.25 0 0
CUI: C3839044
Disease: Compensated liver disease
Compensated liver disease 		4 0 1 0.25 0 0
CUI: C4552187
Disease: Cardiac iron overload
Cardiac iron overload 		4 0 1 0.25 0 0
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 0 1 0.20 0 0
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		5 0 1 0.20 0 0
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 0 1 0.17 0 0
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		6 0 1 0.17 0 0