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: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 9.6E-03 0 0
CUI: C4023528
Disease: Abnormality of skin morphology
Abnormality of skin morphology 		16 0 1 6.2E-02 0 0
CUI: C0023440
Disease: Acute Erythroblastic Leukemia
Acute Erythroblastic Leukemia 		302 0 1 3.3E-03 0 0
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia 		236 0 1 4.2E-03 0 0
CUI: C0023493
Disease: Adult T-Cell Lymphoma/Leukemia
Adult T-Cell Lymphoma/Leukemia 		540 0 1 1.9E-03 0 0
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 1 3.7E-02 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		1758 0 1 5.7E-04 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 1 5.0E-02 0 0
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		182 0 1 5.5E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 3.1E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination 		32 0 1 3.1E-02 0 0
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		2832 0 1 3.5E-04 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		5473 0 1 1.8E-04 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0149530
Disease: Congenital heart block
Congenital heart block 		20 0 1 5.0E-02 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		1760 0 1 5.7E-04 0 0
CUI: C0270715
Disease: Degenerative Diseases, Central Nervous System
Degenerative Diseases, Central Nervous System 		43 0 1 2.3E-02 0 0
CUI: C0751733
Disease: Degenerative Diseases, Spinal Cord
Degenerative Diseases, Spinal Cord 		40 0 1 2.5E-02 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 0 1 3.0E-03 0 0
CUI: C0270855
Disease: Early myoclonic encephalopathy
Early myoclonic encephalopathy 		10 0 1 1.0E-01 0 0
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis 		272 0 1 3.7E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 0 1 2.2E-03 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		73 23 1 1.4E-02 1 3.6E-02
CUI: C0014544
Disease: Epilepsy
Epilepsy 		1215 0 1 8.2E-04 0 0