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: C0019114
Disease: Hemosiderosis
Hemosiderosis 		0 2 0 0 1 3.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.4E-03
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 3.4E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 3.4E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 3.4E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 3.4E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.4E-03
CUI: C0334328
Disease: Microfollicular adenoma
Microfollicular adenoma 		0 1 0 0 1 3.4E-03
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 3.2E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 3.4E-03
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 3.2E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.4E-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 3.4E-03
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 3.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.4E-03
CUI: C4225180
Disease: EVEN-PLUS SYNDROME
EVEN-PLUS SYNDROME 		0 5 0 0 1 3.4E-03
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 6.5E-04 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 6.6E-04 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		65 0 1 6.6E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 6.6E-04 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 6.6E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 6.7E-04 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 6.7E-04 0 0