Source: ALL
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 1.3E-03 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		590 0 1 1.4E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 0 1 1.5E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		417 0 1 1.9E-03 0 0
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 0 1 2.0E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck 		288 0 1 2.6E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 0 1 2.6E-03 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		274 0 1 2.7E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		255 0 1 2.8E-03 0 0
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis 		253 0 1 2.8E-03 0 0
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		593 0 2 2.9E-03 0 0
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		593 0 2 2.9E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.9E-03 0 0
CUI: C0007129
Disease: Merkel cell carcinoma
Merkel cell carcinoma 		226 0 1 3.1E-03 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		226 0 1 3.1E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 3.1E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 3.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.1E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 0 3 3.2E-03 0 0
CUI: C0220621
Disease: Childhood Acute Myeloid Leukemia
Childhood Acute Myeloid Leukemia 		215 0 1 3.2E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 3.2E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 3.2E-03 0 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses 		194 0 1 3.4E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		194 0 1 3.4E-03 0 0
CUI: C1858085
Disease: Malar flattening
Malar flattening 		190 0 1 3.4E-03 0 0