Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Dynein arm defect of respiratory motile cilia
3 2 3 0.43 2 1.00
CUI: C3542550
Disease: CILIARY DYSKINESIA, PRIMARY, 17
CILIARY DYSKINESIA, PRIMARY, 17
2 0 2 0.29 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx
13 0 3 0.18 0 0
Other specified congenital malformations of respiratory system
13 0 3 0.18 0 0
CILIARY DYSKINESIA, PRIMARY, 2 (disorder)
1 0 1 0.14 0 0
CUI: C3543826
Disease: CILIARY DYSKINESIA, PRIMARY, 19
CILIARY DYSKINESIA, PRIMARY, 19
1 0 1 0.14 0 0
CUI: C3809543
Disease: CILIARY DYSKINESIA, PRIMARY, 22
CILIARY DYSKINESIA, PRIMARY, 22
1 0 1 0.14 0 0
CUI: C4748052
Disease: CILIARY DYSKINESIA, PRIMARY, 38
CILIARY DYSKINESIA, PRIMARY, 38
1 0 1 0.14 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 6 0.14 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis
35 0 5 0.14 0 0
Respiratory insufficiency due to defective ciliary clearance
10 0 2 0.13 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 5 0.12 0 0
Impaired nasal mucociliary clearance
41 0 5 0.12 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 5 1.0E-01 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy
48 0 5 1.0E-01 0 0
CUI: C0024248
Disease: Lymphocele
Lymphocele
5 0 1 9.1E-02 0 0
CUI: C3889636
Disease: SPINOCEREBELLAR ATAXIA 37
SPINOCEREBELLAR ATAXIA 37
5 0 1 9.1E-02 0 0
Abnormal respiratory motile cilium morphology
5 0 1 9.1E-02 0 0
CUI: C0742857
Disease: Acute cough
Acute cough
6 0 1 8.3E-02 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 402 5 8.2E-02 1 2.5E-03
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 5 7.8E-02 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 5 7.2E-02 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 8 7 6.7E-02 2 0.25
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility
9 5 1 6.7E-02 1 0.17
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
80 0 5 6.1E-02 0 0