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: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 1.9E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 2.0E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 2.3E-03 0 0
Creatine phosphokinase serum increased
228 0 1 2.4E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 2.4E-03 0 0
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
218 0 1 2.4E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 2.4E-03 0 0
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
206 0 1 2.5E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry
206 0 1 2.5E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 2.6E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 2.6E-03 0 0
Small for gestational age (disorder)
181 0 1 2.7E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.7E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.8E-03 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy
156 0 1 2.8E-03 0 0
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus
156 0 1 2.8E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk
156 0 1 2.8E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
152 0 1 2.9E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 2.9E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
146 0 1 2.9E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
145 0 1 2.9E-03 0 0
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
144 0 1 2.9E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 3.0E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
138 0 1 3.0E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
136 0 1 3.0E-03 0 0