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 3.0E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 1 2.9E-03
CUI: C0543754
Disease: Klinefelter Syndrome, Variants
Klinefelter Syndrome, Variants
0 1 0 0 1 3.0E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 3.0E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.0E-03
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 3.0E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 2.9E-03
CUI: C0079504
Disease: Hermanski-Pudlak Syndrome
Hermanski-Pudlak Syndrome
70 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
Aspartate aminotransferase measurement
57 0 1 1.3E-03 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
57 0 1 1.3E-03 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 1.3E-03 0 0
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
51 0 1 1.3E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
50 0 1 1.3E-03 0 0
CUI: C0549297
Disease: Auricular swelling
Auricular swelling
49 0 1 1.3E-03 0 0
Childhood Acute Megakaryoblastic Leukemia
45 0 1 1.3E-03 0 0
CUI: C0234860
Disease: Weak cry
Weak cry
42 0 1 1.3E-03 0 0
Alanine aminotransferase measurement
41 0 1 1.3E-03 0 0
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia
41 0 1 1.3E-03 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia
41 0 1 1.3E-03 0 0
Serum Alanine Aminotransferase Measurement
41 0 1 1.3E-03 0 0
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
41 0 1 1.3E-03 0 0
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy
40 0 1 1.3E-03 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 1 1.3E-03 0 0