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: C0079683
Disease: Herlitz Disease
Herlitz Disease 		0 197 0 0 1 4.8E-03
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 9.1E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 9.1E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 2 0.13
CUI: C0268374
Disease: Adult junctional epidermolysis bullosa (disorder)
Adult junctional epidermolysis bullosa (disorder) 		0 35 0 0 1 2.2E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 9.1E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 7.1E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0 35 0 0 1 2.2E-02
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 9.1E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 7.7E-02
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		0 1 0 0 1 9.1E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 8.3E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0 35 0 0 1 2.2E-02
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 7.7E-02
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		0 1 0 0 1 9.1E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		0 1 0 0 1 9.1E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 2 0.18
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		0 1 0 0 1 9.1E-02
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 2 0.18
CUI: C4011403
Disease: AMELOGENESIS IMPERFECTA, TYPE IA
AMELOGENESIS IMPERFECTA, TYPE IA 		0 9 0 0 1 5.3E-02
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.0E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 2.0E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.0E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 2.0E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 344 1 2.1E-03 1 2.8E-03