Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Corpuscular Hemoglobin Concentration Mean
401 0 1 2.0E-03 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 1 2.7E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 0 1 2.8E-03 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus
269 0 1 2.8E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.8E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 2.8E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
255 0 1 2.9E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 2.9E-03 0 0
CUI: C4277690
Disease: Ciliopathies
Ciliopathies
241 0 1 3.0E-03 0 0
CUI: C2347747
Disease: Adult Classical Hodgkin Lymphoma
Adult Classical Hodgkin Lymphoma
233 0 1 3.1E-03 0 0
Creatine phosphokinase serum increased
228 0 1 3.2E-03 0 0
CUI: C1306837
Disease: Papillary Renal Cell Carcinoma
Papillary Renal Cell Carcinoma
223 0 1 3.2E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 3.2E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 3.4E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 3.4E-03 0 0
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
197 0 1 3.5E-03 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration
195 0 1 3.5E-03 0 0
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
188 0 1 3.6E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index
1014 0 4 3.6E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 1 3.7E-03 0 0
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
183 0 1 3.7E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 0 1 3.7E-03 0 0
CUI: C0080178
Disease: Spina Bifida
Spina Bifida
179 0 1 3.7E-03 0 0
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease
179 0 1 3.7E-03 0 0
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis
176 0 1 3.8E-03 0 0