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: C0024248
Disease: Lymphocele
Lymphocele 		5 0 2 0.25 0 0
CUI: C0742857
Disease: Acute cough
Acute cough 		6 0 2 0.22 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 3 0.20 0 0
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		13 0 3 0.20 0 0
CUI: C1837618
Disease: CILIARY DYSKINESIA, PRIMARY, 3
CILIARY DYSKINESIA, PRIMARY, 3 		1 26 1 0.20 1 3.7E-02
CUI: C2675867
Disease: CILIARY DYSKINESIA, PRIMARY, 10
CILIARY DYSKINESIA, PRIMARY, 10 		1 0 1 0.20 0 0
CUI: C3542550
Disease: CILIARY DYSKINESIA, PRIMARY, 17
CILIARY DYSKINESIA, PRIMARY, 17 		2 0 1 0.17 0 0
CUI: C4022990
Disease: Dynein arm defect of respiratory motile cilia
Dynein arm defect of respiratory motile cilia 		3 0 1 0.14 0 0
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis 		15 0 2 0.11 0 0
CUI: C0085650
Disease: Purpura Fulminans
Purpura Fulminans 		15 0 2 0.11 0 0
CUI: C0221028
Disease: Neonatal thrombocytopenia (disorder)
Neonatal thrombocytopenia (disorder) 		15 0 2 0.11 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 4 9.5E-02 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 4 9.5E-02 0 0
CUI: C4022986
Disease: Absent inner and outer dynein arms
Absent inner and outer dynein arms 		7 0 1 9.1E-02 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 402 5 8.5E-02 2 5.0E-03
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 4 8.2E-02 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		48 0 4 8.2E-02 0 0
CUI: C1855669
Disease: Absent frontal sinuses
Absent frontal sinuses 		9 0 1 7.7E-02 0 0
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology 		9 0 1 7.7E-02 0 0
CUI: C0010314
Disease: Cri-du-Chat Syndrome
Cri-du-Chat Syndrome 		11 0 1 6.7E-02 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 3 6.7E-02 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis 		62 0 4 6.3E-02 0 0
CUI: C0020449
Disease: Hyperdistention
Hyperdistention 		12 0 1 6.2E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 2 6.2E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 2 6.2E-02 0 0