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: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 3 30 1.00 2 0.11
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 29 0.97 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 29 0.97 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 29 0.94 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 29 0.72 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 29 0.72 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 7 0.19 0 0
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		13 0 7 0.19 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 6 0.16 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 11 0.14 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 11 0.13 0 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		7 0 4 0.12 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 9 0.12 0 0
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous 		9 0 4 0.11 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 11 0.11 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 7 0.11 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 7 0.11 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 7 0.11 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 13 0.11 0 0
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages 		3 0 3 1.0E-01 0 0
CUI: C1876171
Disease: Polyasplenia
Polyasplenia 		3 0 3 1.0E-01 0 0
CUI: C1876172
Disease: VAH, AUTOSOMAL RECESSIVE
VAH, AUTOSOMAL RECESSIVE 		3 0 3 1.0E-01 0 0
CUI: C1876173
Disease: Heterotaxy, Visceroatrial, Autosomal Recessive
Heterotaxy, Visceroatrial, Autosomal Recessive 		3 0 3 1.0E-01 0 0
CUI: C2910124
Disease: Isomerism of atrial appendages with asplenia or polysplenia
Isomerism of atrial appendages with asplenia or polysplenia 		3 0 3 1.0E-01 0 0
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		14 0 4 1.0E-01 0 0