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: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 30 0.77 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 29 0.74 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 29 0.74 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
30 0 29 0.72 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 29 0.72 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
39 0 29 0.59 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome
13 5 10 0.24 1 8.3E-02
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 16 0.21 0 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome
7 0 7 0.18 0 0
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous
9 0 7 0.17 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx
13 0 7 0.16 0 0
Other specified congenital malformations of respiratory system
13 0 7 0.16 0 0
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism
6 0 6 0.15 0 0
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism
14 0 7 0.15 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 11 0.13 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 16 0.13 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 11 0.12 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
80 0 12 0.11 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen
41 0 8 0.11 0 0
CUI: C0392482
Disease: Common atrium
Common atrium
11 0 5 0.11 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia
15 0 5 0.10 0 0
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
61 18 9 9.9E-02 1 4.0E-02
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 7 9.6E-02 0 0
Impaired nasal mucociliary clearance
41 0 7 9.6E-02 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 7 8.7E-02 0 0