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: C0220810
Disease: Congenital defects
Congenital defects 		126 0 1 7.9E-03 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		406 0 1 2.5E-03 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 3.3E-02 0 0
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		267 0 1 3.7E-03 0 0
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		1576 0 1 6.3E-04 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		234 0 1 4.3E-03 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis 		54 0 1 1.9E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		30 0 1 3.3E-02 0 0
CUI: C0011991
Disease: Diarrhea
Diarrhea 		632 0 1 1.6E-03 0 0
CUI: C0729233
Disease: Dissecting aneurysm of the thoracic aorta
Dissecting aneurysm of the thoracic aorta 		57 0 1 1.8E-02 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 2.1E-02 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		222 0 1 4.5E-03 0 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney 		27 0 1 3.7E-02 0 0
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		109 0 1 9.2E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 1 1.2E-03 0 0
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 0 1 9.3E-04 0 0
CUI: C0746883
Disease: Febrile Neutropenia
Febrile Neutropenia 		58 0 1 1.7E-02 0 0
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		21 0 1 4.8E-02 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 1 1.3E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 2.6E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.3E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 1 2.6E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.4E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.4E-02 0 0
CUI: C3495537
Disease: Heterotaxy, Visceral, 5, Autosomal
Heterotaxy, Visceral, 5, Autosomal 		2 0 1 0.50 0 0