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: C1519346
Disease: Skin Carcinogenesis
Skin Carcinogenesis
194 0 1 2.3E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 1 2.3E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 2.3E-03 0 0
CUI: C0151526
Disease: Premature Birth
Premature Birth
192 0 1 2.4E-03 0 0
CUI: C0243038
Disease: Carcinoma, Lewis Lung
Carcinoma, Lewis Lung
188 0 1 2.4E-03 0 0
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
186 0 1 2.4E-03 0 0
CUI: C0205647
Disease: Follicular adenoma
Follicular adenoma
183 0 1 2.4E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
182 0 1 2.4E-03 0 0
Malformations of Cortical Development, Group II
180 0 1 2.4E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.4E-03 0 0
CUI: C0029882
Disease: Otitis Media
Otitis Media
175 0 1 2.5E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes
171 0 1 2.5E-03 0 0
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder
171 0 1 2.5E-03 0 0
CUI: C3887499
Disease: Renal cyst
Renal cyst
170 0 1 2.5E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 2.5E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 2.5E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 2.5E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.5E-03 0 0
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
166 0 1 2.5E-03 0 0
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
166 0 1 2.5E-03 0 0
CUI: C0030421
Disease: Paraganglioma
Paraganglioma
165 0 1 2.5E-03 0 0
CUI: C0030499
Disease: Parasitic Diseases
Parasitic Diseases
164 0 1 2.5E-03 0 0
CUI: C0334583
Disease: Pilocytic Astrocytoma
Pilocytic Astrocytoma
163 0 1 2.5E-03 0 0
Collecting Duct Carcinoma of the Kidney
162 0 1 2.5E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 2.5E-03 0 0