Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Congenital hypoplasia of aortic arch
4 1 3 0.33 1 0.50
CUI: C0036400
Disease: Scimitar Syndrome
Scimitar Syndrome
2 1 2 0.25 1 0.50
CUI: C1735886
Disease: Bland White Garland Syndrome
Bland White Garland Syndrome
2 0 2 0.25 0 0
CUI: C4748946
Disease: CARDIAC-UROGENITAL SYNDROME
CARDIAC-UROGENITAL SYNDROME
2 7 2 0.25 1 0.12
Total Anomalous Pulmonary Venous Return 1
3 0 2 0.22 0 0
CUI: C0685707
Disease: Muscular ventricular septum defect
Muscular ventricular septum defect
9 4 3 0.21 1 0.20
CUI: C0221215
Disease: Common atrioventricular canal
Common atrioventricular canal
4 0 2 0.20 0 0
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement
4 0 2 0.20 0 0
Abnormality of chromosome segregation
5 0 2 0.18 0 0
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
9 0 2 0.13 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart
1 0 1 0.12 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur
1 0 1 0.12 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY
1 0 1 0.12 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve
1 0 1 0.12 0 0
CUI: C0266357
Disease: Persistent umbilical sinus
Persistent umbilical sinus
1 0 1 0.12 0 0
CUI: C0267581
Disease: Rectal Stenosis
Rectal Stenosis
1 0 1 0.12 0 0
CUI: C0339675
Disease: Axial hypermetropia
Axial hypermetropia
1 0 1 0.12 0 0
CUI: C0344923
Disease: Multiple ventricular septal defects
Multiple ventricular septal defects
1 0 1 0.12 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism
1 0 1 0.12 0 0
Osteoarthritis of glenohumeral joint
1 0 1 0.12 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing
1 0 1 0.12 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares
1 0 1 0.12 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis
1 0 1 0.12 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx
1 0 1 0.12 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III
1 0 1 0.12 0 0