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: C1836193
Disease: Synostosis of carpal bones
Synostosis of carpal bones
23 0 6 8.3E-02 0 0
Ostium secundum atrial septal defect
37 0 7 8.2E-02 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine
77 0 10 8.2E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
384 96 33 8.1E-02 1 9.2E-03
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis
106 0 12 8.1E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 7 8.0E-02 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs
13 0 5 7.9E-02 0 0
CUI: C0578038
Disease: Thin lips
Thin lips
99 0 11 7.7E-02 0 0
CUI: C0521620
Disease: Dilatation of ureter
Dilatation of ureter
72 0 9 7.6E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia
30 0 6 7.6E-02 0 0
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia
59 0 8 7.5E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 7 7.5E-02 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
274 0 23 7.5E-02 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur
31 0 6 7.5E-02 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes
61 0 8 7.4E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 87 33 7.4E-02 1 1.0E-02
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects
77 0 9 7.3E-02 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
92 0 10 7.3E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux
48 0 7 7.3E-02 0 0
Partial defect of atrioventricular canal
4 0 4 7.3E-02 0 0
CUI: C4531220
Disease: Coronary sinus enlargement
Coronary sinus enlargement
4 0 4 7.3E-02 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome
20 0 5 7.1E-02 0 0
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism
6 0 4 7.0E-02 0 0
CUI: C4023170
Disease: Abnormal oral mucosa morphology
Abnormal oral mucosa morphology
6 0 4 7.0E-02 0 0
CUI: C0265783
Disease: Congenital hypoplasia of lung
Congenital hypoplasia of lung
175 0 15 7.0E-02 0 0