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: C0037369
Disease: Smoking
Smoking 		391 0 1 1.9E-03 0 0
CUI: C0017152
Disease: Gastritis
Gastritis 		292 0 1 2.4E-03 0 0
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		284 0 1 2.4E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.5E-03 0 0
CUI: C0333463
Disease: Senile Plaques
Senile Plaques 		249 0 1 2.7E-03 0 0
CUI: C2347747
Disease: Adult Classical Hodgkin Lymphoma
Adult Classical Hodgkin Lymphoma 		233 0 1 2.8E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.8E-03 0 0
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection 		219 0 1 2.9E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.9E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.9E-03 0 0
CUI: C0023827
Disease: liposarcoma
liposarcoma 		200 0 1 3.1E-03 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 0 1 3.1E-03 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		192 0 1 3.1E-03 0 0
CUI: C0876973
Disease: Infectious Lung Disorder
Infectious Lung Disorder 		185 0 1 3.2E-03 0 0
CUI: C0017185
Disease: Gastrointestinal Neoplasms
Gastrointestinal Neoplasms 		182 0 1 3.2E-03 0 0
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		181 0 1 3.2E-03 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 1 3.3E-03 0 0
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		177 0 1 3.3E-03 0 0
CUI: C4048158
Disease: Convulsions
Convulsions 		174 0 1 3.3E-03 0 0
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		173 0 1 3.3E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.3E-03 0 0
CUI: C0085633
Disease: Mood swings
Mood swings 		171 0 1 3.4E-03 0 0
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder 		171 0 1 3.4E-03 0 0
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		168 0 1 3.4E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 3.4E-03 0 0