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: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 6.6E-03 0 0
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		182 0 1 5.5E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 5.3E-03 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 0 1 5.1E-03 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		230 0 1 4.3E-03 0 0
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia 		236 0 1 4.2E-03 0 0
CUI: C4520840
Disease: Erythroleukemia (Erythroid/Myeloid)
Erythroleukemia (Erythroid/Myeloid) 		237 0 1 4.2E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 0 1 3.8E-03 0 0
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis 		272 0 1 3.7E-03 0 0
CUI: C0023440
Disease: Acute Erythroblastic Leukemia
Acute Erythroblastic Leukemia 		302 0 1 3.3E-03 0 0
CUI: C0151449
Disease: Primary Sjögren's syndrome
Primary Sjögren's syndrome 		312 0 1 3.2E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 3.1E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 3.1E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 0 1 3.0E-03 0 0
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		360 0 1 2.8E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.6E-03 0 0
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		394 0 1 2.5E-03 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		429 0 1 2.3E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C0023492
Disease: Leukemia, T-Cell
Leukemia, T-Cell 		457 0 1 2.2E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 0 1 2.2E-03 0 0
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome 		481 0 1 2.1E-03 0 0
CUI: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage 		501 0 1 2.0E-03 0 0
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		512 0 1 2.0E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		539 0 1 1.9E-03 0 0