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: C0018862
Disease: Heberden node
Heberden node 		0 1 0 0 1 1.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.3E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 1.3E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 2 2.5E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 1.3E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.3E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0 35 0 0 1 9.0E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 1.3E-02
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 1.3E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 2.6E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 1.3E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 1.3E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 2 2.6E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0 35 0 0 1 9.0E-03
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		0 20 0 0 1 1.0E-02
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		0 1 0 0 1 1.3E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		0 1 0 0 1 1.3E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 2 2.6E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		0 1 0 0 1 1.3E-02
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 2 2.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.3E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.3E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.5E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 1.4E-03 0 0