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: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 13 1.00 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 13 0.32 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 13 0.32 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 13 0.27 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		48 0 13 0.27 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 9 0.23 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 13 0.22 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 10 0.22 0 0
CUI: C3552099
Disease: Respiratory insufficiency due to defective ciliary clearance
Respiratory insufficiency due to defective ciliary clearance 		10 0 4 0.21 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis 		62 0 13 0.21 0 0
CUI: C0024248
Disease: Lymphocele
Lymphocele 		5 0 3 0.20 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 7 0.20 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 7 0.20 0 0
CUI: C4025100
Disease: Abnormal respiratory motile cilium morphology
Abnormal respiratory motile cilium morphology 		5 0 3 0.20 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 7 0.19 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 7 0.19 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 7 0.19 0 0
CUI: C0742857
Disease: Acute cough
Acute cough 		6 0 3 0.19 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 12 0.18 0 0
CUI: C4022986
Disease: Absent inner and outer dynein arms
Absent inner and outer dynein arms 		7 0 3 0.18 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 13 0.16 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 13 0.16 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 7 0.16 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 7 0.16 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers 		88 0 13 0.15 0 0