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: C1305855
Disease: Body mass index
Body mass index
1014 0 1 9.0E-04 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.4E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 2.8E-03 0 0
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies
271 0 1 2.8E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 2.9E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.0E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 1 3.1E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 3.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 3 3.2E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 3.2E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 3.2E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 3.3E-03 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
210 0 1 3.3E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 3.5E-03 0 0
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
191 0 1 3.5E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 3.6E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 3.6E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 3.8E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 3.8E-03 0 0
Flexion contracture of proximal interphalangeal joint
168 0 1 3.9E-03 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness
163 0 1 3.9E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
163 0 1 3.9E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 4.0E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head
154 0 1 4.1E-03 0 0