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: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		0 3 0 0 1 2.2E-02
CUI: C0018862
Disease: Heberden node
Heberden node 		0 1 0 0 1 2.3E-02
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric 		0 4 0 0 1 2.2E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 2.3E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 2.3E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 2.1E-02
CUI: C0337439
Disease: Iron measurement
Iron measurement 		0 16 0 0 1 1.7E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 2.1E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 1.6E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		0 16 0 0 1 1.7E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 1.6E-02
CUI: C0855247
Disease: Sleep attack
Sleep attack 		0 3 0 0 1 2.2E-02
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 2.3E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 2.2E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0 25 0 0 1 1.5E-02
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		0 20 0 0 1 1.6E-02
CUI: C1968782
Disease: MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES 		0 4 0 0 1 2.2E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0 26 0 0 1 1.5E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 1 2.3E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		0 3 0 0 1 2.2E-02
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		0 16 0 0 1 1.7E-02
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 2.3E-02
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		0 2 0 0 1 2.3E-02
CUI: C4016398
Disease: COSTELLO SYNDROME, SEVERE
COSTELLO SYNDROME, SEVERE 		0 1 0 0 1 2.3E-02
CUI: C4302205
Disease: Neonatal thrombosis of cerebral venous sinus
Neonatal thrombosis of cerebral venous sinus 		0 2 0 0 1 2.3E-02