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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.8E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.8E-03
CUI: C1095928
Disease: Secondary hyperthyroidism
Secondary hyperthyroidism 		0 1 0 0 1 2.8E-03
CUI: C1299432
Disease: Multi vessel coronary artery disease
Multi vessel coronary artery disease 		0 1 0 0 1 2.8E-03
CUI: C1318233
Disease: immunoglobulin G index
immunoglobulin G index 		0 4 0 0 1 2.8E-03
CUI: C1446147
Disease: IgG Index (procedure)
IgG Index (procedure) 		0 4 0 0 1 2.8E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 2.8E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 2.8E-03
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 2.8E-03
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0 46 0 0 3 7.6E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.8E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 2.8E-03
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 1.7E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		5 0 1 1.7E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis 		4 0 1 1.7E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 1.7E-03 0 0
CUI: C0001338
Disease: Herpetic Acute Necrotizing Encephalitis
Herpetic Acute Necrotizing Encephalitis 		5 0 1 1.7E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 1.7E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 1.7E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		61 0 1 1.6E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder 		6 0 1 1.7E-03 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity 		2 0 1 1.7E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis 		1 0 1 1.7E-03 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		16 0 1 1.7E-03 0 0