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 0.33 0 0
CUI: C2673913
Disease: Anemia, Hypochromic Microcytic, With Iron Overload
Anemia, Hypochromic Microcytic, With Iron Overload 		4 0 3 0.33 0 0
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 3 0.33 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 4 0.29 0 0
CUI: C1833296
Disease: FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED 		6 0 3 0.27 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 2 0.25 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 3 0.23 0 0
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 0 2 0.22 0 0
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 2 0.22 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 0 2 0.20 0 0
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		6 0 2 0.17 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 0 5 0.15 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 3 0.15 0 0
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis 		8 0 2 0.14 0 0
CUI: C1851400
Disease: Facial Hypertrichosis
Facial Hypertrichosis 		8 0 2 0.14 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 0 4 0.13 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 0.12 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 0.12 0 0
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 2 0.12 0 0
CUI: C0152516
Disease: Bacterial enteritis
Bacterial enteritis 		1 0 1 0.12 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 0.12 0 0
CUI: C0264134
Disease: Hallux Rigidus
Hallux Rigidus 		1 0 1 0.12 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 0.12 0 0
CUI: C0275553
Disease: Bacterial cholangitis
Bacterial cholangitis 		1 0 1 0.12 0 0
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
Hypocalciuric hypercalcemia, familial, type 1 		46 0 6 0.12 0 0