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: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
0 1 0 0 1 2.1E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 2.1E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda
0 6 0 0 1 1.9E-02
CUI: C0337439
Disease: Iron measurement
Iron measurement
0 16 0 0 1 1.6E-02
CUI: C0428578
Disease: Iron level result
Iron level result
0 16 0 0 1 1.6E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 2.0E-02
Diastolic blood pressure measurement
0 81 0 0 1 7.8E-03
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0 95 0 0 1 7.0E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 2.1E-02
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3
0 20 0 0 1 1.5E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0 26 0 0 1 1.4E-02
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
0 2 0 0 1 2.0E-02
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
0 2 0 0 1 2.0E-02
Frequent episodic tension-type headache
0 1 0 0 1 2.1E-02
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
90 0 1 1.2E-03 0 0
Autosomal recessive retinitis pigmentosa
82 0 1 1.2E-03 0 0
CUI: C0240912
Disease: Vertical Talus
Vertical Talus
69 0 1 1.2E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result
65 0 1 1.2E-03 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 0 1 1.2E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
62 0 1 1.2E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
62 0 1 1.2E-03 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 1 1.2E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 1.2E-03 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia
59 0 1 1.2E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 1 1.2E-03 0 0