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: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 3 1 0.20 1 0.20
CUI: C1851400
Disease: Facial Hypertrichosis
Facial Hypertrichosis 		8 0 2 0.20 0 0
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 3 1 0.20 1 0.20
CUI: C2931746
Disease: Sulfocysteinuria
Sulfocysteinuria 		2 0 1 0.20 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 0.20 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 0.20 0 0
CUI: C0162569
Disease: Hepatoerythropoietic Porphyria
Hepatoerythropoietic Porphyria 		3 0 1 0.17 0 0
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		3 1 1 0.17 1 0.33
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 20 1 0.17 2 9.5E-02
CUI: C4552431
Disease: Complicated urinary tract infection
Complicated urinary tract infection 		3 0 1 0.17 0 0
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		4 2 1 0.14 2 0.67
CUI: C1839167
Disease: Intermittent thrombocytopenia
Intermittent thrombocytopenia 		4 0 1 0.14 0 0
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 1 0.14 0 0
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 1 0.14 0 0
CUI: C3839044
Disease: Compensated liver disease
Compensated liver disease 		4 0 1 0.14 0 0
CUI: C4552187
Disease: Cardiac iron overload
Cardiac iron overload 		4 0 1 0.14 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 39 4 0.13 3 7.7E-02
CUI: C0020058
Disease: Howell-Jolly Bodies
Howell-Jolly Bodies 		5 0 1 0.12 0 0
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 4 1 0.12 1 0.17
CUI: C0795856
Disease: Trisomy 15
Trisomy 15 		5 0 1 0.12 0 0
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		5 1 1 0.12 1 0.33
CUI: C1859690
Disease: CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME 		5 0 1 0.12 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 2 0.12 2 0.50
CUI: C0085661
Disease: Onycholysis
Onycholysis 		15 0 2 0.12 0 0
CUI: C0037997
Disease: Splenic Diseases
Splenic Diseases 		6 0 1 0.11 0 0