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 		15 0 4 0.19 0 0
CUI: C0854279
Disease: Basal ganglion degeneration
Basal ganglion degeneration 		3 0 2 0.18 0 0
CUI: C1848030
Disease: Hypotonia-Cystinuria Syndrome
Hypotonia-Cystinuria Syndrome 		6 0 2 0.14 0 0
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis 		8 0 2 0.12 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 2 0.12 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 1.0E-01 0 0
CUI: C0152516
Disease: Bacterial enteritis
Bacterial enteritis 		1 0 1 1.0E-01 0 0
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 3 1.0E-01 0 0
CUI: C0275553
Disease: Bacterial cholangitis
Bacterial cholangitis 		1 0 1 1.0E-01 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 1.0E-01 0 0
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		1 0 1 1.0E-01 0 0
CUI: C1862229
Disease: Adult i Blood Group Phenotype
Adult i Blood Group Phenotype 		1 0 1 1.0E-01 0 0
CUI: C1865616
Disease: HEMOCHROMATOSIS, TYPE 2B
HEMOCHROMATOSIS, TYPE 2B 		1 0 1 1.0E-01 0 0
CUI: C2677608
Disease: Thrombocytopenia 4
Thrombocytopenia 4 		1 0 1 1.0E-01 0 0
CUI: C3489571
Disease: Familial Extrahepatic Biliary Atresia
Familial Extrahepatic Biliary Atresia 		1 0 1 1.0E-01 0 0
CUI: C3489572
Disease: Idiopathic Extrahepatic Biliary Atresia
Idiopathic Extrahepatic Biliary Atresia 		1 0 1 1.0E-01 0 0
CUI: C3805373
Disease: CATARACT 13 WITH ADULT i PHENOTYPE
CATARACT 13 WITH ADULT i PHENOTYPE 		1 0 1 1.0E-01 0 0
CUI: C3810090
Disease: L-FERRITIN DEFICIENCY
L-FERRITIN DEFICIENCY 		1 0 1 1.0E-01 0 0
CUI: C4016051
Disease: L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE
L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C4017428
Disease: CERULOPLASMIN BELFAST PHENOTYPE
CERULOPLASMIN BELFAST PHENOTYPE 		1 0 1 1.0E-01 0 0
CUI: C4024952
Disease: Cavitation of the basal ganglia
Cavitation of the basal ganglia 		1 0 1 1.0E-01 0 0
CUI: C4707880
Disease: Genetic hyperferritinemia without iron overload
Genetic hyperferritinemia without iron overload 		1 0 1 1.0E-01 0 0
CUI: C0029810
Disease: Other specified iron deficiency anemias
Other specified iron deficiency anemias 		13 0 2 9.5E-02 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		26 0 3 9.1E-02 0 0
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 1 9.1E-02 0 0