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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.2E-02
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0 61 0 0 1 7.0E-03
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 1.1E-02
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		0 97 0 0 1 5.6E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.2E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 1.2E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.2E-02
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis 		1 0 1 7.9E-03 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output 		1 0 1 7.9E-03 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 7.9E-03 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced 		1 0 1 7.9E-03 0 0
CUI: C0015338
Disease: Exstrophy
Exstrophy 		1 0 1 7.9E-03 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 7.9E-03 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 7.9E-03 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 7.9E-03 0 0
CUI: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 7.9E-03 0 0
CUI: C0023869
Disease: Lithiasis
Lithiasis 		1 0 1 7.9E-03 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis 		1 0 1 7.9E-03 0 0
CUI: C0039870
Disease: Thinness
Thinness 		1 0 1 7.9E-03 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 7.9E-03 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 7.9E-03 0 0
CUI: C0149662
Disease: Deformity of toe
Deformity of toe 		1 0 1 7.9E-03 0 0
CUI: C0154738
Disease: Lumbosacral radiculopathy
Lumbosacral radiculopathy 		1 0 1 7.9E-03 0 0