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: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.4E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.8E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 2.0E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
362 0 1 2.3E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.5E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 2 2.8E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck
288 0 1 2.8E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.9E-03 0 0
Red cell distribution width determination
593 0 2 3.0E-03 0 0
RDW - Red blood cell distribution width result
593 0 2 3.0E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.1E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 3.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 3 3.2E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 3.3E-03 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
234 0 1 3.3E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 3.3E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia
218 0 1 3.4E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 3.5E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 3.5E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
213 0 1 3.5E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead
211 0 1 3.5E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 7 3.6E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 3.6E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 3.6E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 3.7E-03 0 0