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: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 4 0.12 0 0
CUI: C1866091
Disease: Left-Right Axis Malformations
Left-Right Axis Malformations 		2 0 1 0.12 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 4 0.12 0 0
CUI: C3151221
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 		2 0 1 0.12 0 0
CUI: C4015619
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC, 8
EPILEPSY, PROGRESSIVE MYOCLONIC, 8 		2 0 1 0.12 0 0
CUI: C4023237
Disease: Interrupted inferior vena cava with azygous continuation
Interrupted inferior vena cava with azygous continuation 		2 0 1 0.12 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 4 0.12 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 4 0.12 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 4 0.12 0 0
CUI: C1970501
Disease: Hypoplastic pulmonary veins
Hypoplastic pulmonary veins 		3 0 1 0.11 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 6 0.11 0 0
CUI: C0265857
Disease: Uhl anomaly
Uhl anomaly 		4 0 1 1.0E-01 0 0
CUI: C1861235
Disease: Forebrain Defects
Forebrain Defects 		4 0 1 1.0E-01 0 0
CUI: C4082954
Disease: Hypoplasia of right ventricle
Hypoplasia of right ventricle 		4 0 1 1.0E-01 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 4 9.5E-02 0 0
CUI: C4551903
Disease: Total anomalous pulmonary venous return
Total anomalous pulmonary venous return 		16 0 2 9.5E-02 0 0
CUI: C0694453
Disease: Neurotic, stress-related and somatoform disorders
Neurotic, stress-related and somatoform disorders 		5 0 1 9.1E-02 0 0
CUI: C1282979
Disease: Transient hypoparathyroidism
Transient hypoparathyroidism 		5 0 1 9.1E-02 0 0
CUI: C0265908
Disease: Congenital atresia of pulmonary artery
Congenital atresia of pulmonary artery 		19 0 2 8.3E-02 0 0
CUI: C1389016
Disease: ATRIOVENTRICULAR CANAL DEFECT
ATRIOVENTRICULAR CANAL DEFECT 		55 0 4 6.9E-02 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 3 6.7E-02 0 0
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		61 0 4 6.2E-02 0 0
CUI: C4684942
Disease: Refractory Thyroid Gland Carcinoma
Refractory Thyroid Gland Carcinoma 		10 0 1 6.2E-02 0 0
CUI: C0242855
Disease: Congenital atresia of pulmonary valve
Congenital atresia of pulmonary valve 		11 0 1 5.9E-02 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 3 5.8E-02 0 0