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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 8.7E-03
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 8.7E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 8.7E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 8.7E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 8.7E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 8.6E-03
CUI: C1282365
Disease: Mixed type cataract
Mixed type cataract
0 1 0 0 1 8.7E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 8.7E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 8.5E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 8.7E-03
Philadelphia positive acute lymphocytic leukaemia
0 1 0 0 1 8.7E-03
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia
0 2 0 0 2 1.7E-02
CUI: C1445953
Disease: Poor eye contact
Poor eye contact
73 0 1 8.0E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 8.1E-04 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 0 1 8.1E-04 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
62 0 1 8.1E-04 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
62 0 1 8.1E-04 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 8.1E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 8.1E-04 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 1 8.1E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 8.1E-04 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 1 8.2E-04 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
54 0 1 8.2E-04 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 8.2E-04 0 0
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies
53 0 1 8.2E-04 0 0