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: C0852336
Disease: Immune Hemolytic Anemia
Immune Hemolytic Anemia 		3 0 3 0.50 0 0
CUI: C1300128
Disease: Villitis of unknown etiology
Villitis of unknown etiology 		3 0 3 0.50 0 0
CUI: C0920163
Disease: Idiopathic thrombocytopenia
Idiopathic thrombocytopenia 		2 0 2 0.33 0 0
CUI: C1333843
Disease: Grade 3 Invasive Breast Carcinoma
Grade 3 Invasive Breast Carcinoma 		3 0 2 0.29 0 0
CUI: C0154051
Disease: Hemangioma of retina
Hemangioma of retina 		4 0 2 0.25 0 0
CUI: C2973529
Disease: Leukocytoclastic vasculitis
Leukocytoclastic vasculitis 		11 0 3 0.21 0 0
CUI: C0339229
Disease: Superior limbic keratoconjunctivitis
Superior limbic keratoconjunctivitis 		6 0 2 0.20 0 0
CUI: C0017567
Disease: Gingival Hypertrophy
Gingival Hypertrophy 		7 0 2 0.18 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 0.17 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 0.17 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 0.17 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.17 0 0
CUI: C0877016
Disease: Heparin-induced thrombocytopenia type II
Heparin-induced thrombocytopenia type II 		1 0 1 0.17 0 0
CUI: C1096189
Disease: Type II hypersensitivity
Type II hypersensitivity 		1 0 1 0.17 0 0
CUI: C1290590
Disease: Hyperplastic tooth follicle
Hyperplastic tooth follicle 		1 0 1 0.17 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 0 1 0.17 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 0.17 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.17 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 0 1 0.17 0 0
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		16 0 3 0.16 0 0
CUI: C0878693
Disease: Conjunctivochalasis
Conjunctivochalasis 		9 0 2 0.15 0 0
CUI: C0079136
Disease: Cockayne-Touraine Disease
Cockayne-Touraine Disease 		2 0 1 0.14 0 0
CUI: C0151436
Disease: Vasculitis, Leukocytoclastic, Cutaneous
Vasculitis, Leukocytoclastic, Cutaneous 		18 0 3 0.14 0 0