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: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis 		11 0 1 5.6E-02 0 0
CUI: C0006384
Disease: Bundle-Branch Block
Bundle-Branch Block 		12 0 1 5.3E-02 0 0
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		13 22 1 5.0E-02 1 3.1E-02
CUI: C0151516
Disease: Thyroid Hypoplasia
Thyroid Hypoplasia 		14 6 1 4.8E-02 1 6.2E-02
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		39 0 2 4.4E-02 0 0
CUI: C0685889
Disease: Splenic Hypoplasia
Splenic Hypoplasia 		18 0 1 4.0E-02 0 0
CUI: C0012242
Disease: Digestive System Disorders
Digestive System Disorders 		19 0 1 3.8E-02 0 0
CUI: C0856748
Disease: Aneurysm of aortic arch
Aneurysm of aortic arch 		20 0 1 3.7E-02 0 0
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		22 0 1 3.4E-02 0 0
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis 		24 5 1 3.2E-02 1 6.7E-02
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation 		25 0 1 3.1E-02 0 0
CUI: C1836653
Disease: Ascending aortic dissection
Ascending aortic dissection 		25 0 1 3.1E-02 0 0
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		26 0 1 3.0E-02 0 0
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		26 0 1 3.0E-02 0 0
CUI: C0265264
Disease: Holt-Oram syndrome
Holt-Oram syndrome 		28 0 1 2.9E-02 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 1 2.9E-02 0 0
CUI: C3495549
Disease: Patent ductus arteriosus - persisting type
Patent ductus arteriosus - persisting type 		30 10 1 2.7E-02 1 5.0E-02
CUI: C0018808
Disease: Heart murmur
Heart murmur 		31 0 1 2.6E-02 0 0
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		32 0 1 2.6E-02 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 0 1 2.5E-02 0 0
CUI: C0431109
Disease: Choroid Plexus Carcinoma
Choroid Plexus Carcinoma 		34 0 1 2.4E-02 0 0
CUI: C0856747
Disease: Aneurysm of ascending aorta
Aneurysm of ascending aorta 		34 0 1 2.4E-02 0 0
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology 		34 0 1 2.4E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 1 2.4E-02 0 0
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		37 0 1 2.3E-02 0 0