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: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine
77 0 8 6.7E-02 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome
46 0 6 6.6E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 5 6.5E-02 0 0
CUI: C0376175
Disease: Bell Palsy
Bell Palsy
15 0 4 6.5E-02 0 0
CUI: C0008412
Disease: Choline Deficiency
Choline Deficiency
16 0 4 6.3E-02 0 0
CUI: C0338437
Disease: Neurocysticercosis
Neurocysticercosis
34 0 5 6.2E-02 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME
18 0 4 6.2E-02 0 0
CUI: C1861869
Disease: Underdeveloped supraorbital ridges
Underdeveloped supraorbital ridges
53 0 6 6.1E-02 0 0
Slow acetylator due to N-acetyltransferase enzyme variant
20 8 4 6.0E-02 1 1.9E-02
CUI: C0795822
Disease: Recombinant chromosome 8 syndrome
Recombinant chromosome 8 syndrome
3 0 3 5.9E-02 0 0
CUI: C4016400
Disease: LUNG CANCER, SOMATIC
LUNG CANCER, SOMATIC
3 0 3 5.9E-02 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
274 83 18 5.9E-02 5 4.1E-02
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia
59 0 6 5.8E-02 0 0
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle
4 1 3 5.8E-02 1 2.2E-02
CUI: C1298680
Disease: Occlusive stroke
Occlusive stroke
4 0 3 5.8E-02 0 0
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia
78 0 7 5.7E-02 0 0
CUI: C0024620
Disease: Primary Malignant Liver Neoplasm
Primary Malignant Liver Neoplasm
60 4 6 5.7E-02 2 4.3E-02
CUI: C1705254
Disease: Neonatal Deformity
Neonatal Deformity
23 0 4 5.7E-02 0 0
CUI: C1852759
Disease: Papillorenal syndrome
Papillorenal syndrome
5 0 3 5.7E-02 0 0
CUI: C0015652
Disease: Fascioliasis
Fascioliasis
24 0 4 5.6E-02 0 0
CUI: C3665629
Disease: Dental fluorosis
Dental fluorosis
24 0 4 5.6E-02 0 0
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association
25 0 4 5.6E-02 0 0
Viral gastroenteritis due to Rotavirus
7 0 3 5.5E-02 0 0
CUI: C0744669
Disease: Complex congenital heart disease
Complex congenital heart disease
7 1 3 5.5E-02 1 2.2E-02
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin
7 0 3 5.5E-02 0 0