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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 7.6E-03
CUI: C0018498
Disease: Hair Color
Hair Color 		0 312 0 0 1 2.3E-03
CUI: C0018862
Disease: Heberden node
Heberden node 		0 1 0 0 1 8.1E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 8.1E-03
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 8.1E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 8.1E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 7.8E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 7.8E-03
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 7.0E-03
CUI: C0599949
Disease: Arterial Stiffness
Arterial Stiffness 		0 1 0 0 1 8.1E-03
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 7.0E-03
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 1 8.1E-03
CUI: C0854740
Disease: Delayed sleep phase
Delayed sleep phase 		0 1 0 0 1 8.1E-03
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0 25 0 0 1 6.8E-03
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 8.1E-03
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		0 20 0 0 1 7.0E-03
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0 26 0 0 1 6.8E-03
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 1 8.1E-03
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 8.1E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 8.1E-03
CUI: C3541318
Disease: Soluble Transferrin Receptor Measurement
Soluble Transferrin Receptor Measurement 		0 7 0 0 1 7.8E-03
CUI: C3553462
Disease: INFLUENZA, SEVERE, SUSCEPTIBILITY TO
INFLUENZA, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 8.1E-03
CUI: C3665951
Disease: Influenza due to Influenza A virus subtype H7N9
Influenza due to Influenza A virus subtype H7N9 		0 3 0 0 1 8.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 8.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 8.0E-03