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 4.9E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 5.1E-03
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric
0 4 0 0 1 5.0E-03
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
0 1 0 0 1 5.1E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 5.1E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda
0 6 0 0 1 5.0E-03
Secondary acquired sideroblastic anemia
0 2 0 0 1 5.1E-03
CUI: C0337439
Disease: Iron measurement
Iron measurement
0 16 0 0 1 4.7E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 5.1E-03
CUI: C0428578
Disease: Iron level result
Iron level result
0 16 0 0 1 4.7E-03
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3
0 20 0 0 1 4.6E-03
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0 26 0 0 1 4.5E-03
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
0 2 0 0 1 5.1E-03
HFE-Associated Hereditary Hemochromatosis
0 3 0 0 1 5.0E-03
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
0 2 0 0 1 5.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 5.0E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 5.1E-03
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 1.1E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
104 0 1 1.2E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 1 1.2E-03 0 0
CUI: C1853241
Disease: Flat face
Flat face
83 0 1 1.2E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 1.2E-03 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
80 0 1 1.2E-03 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease
78 0 1 1.2E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia
77 0 1 1.2E-03 0 0