Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Respiratory insufficiency due to defective ciliary clearance
10 0 10 0.21 0 0
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis
190 0 41 0.21 0 0
CUI: C0149516
Disease: Chronic sinusitis
Chronic sinusitis
205 0 43 0.20 0 0
CUI: C0010200
Disease: Coughing
Coughing
235 0 42 0.17 0 0
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis
15 0 9 0.17 0 0
CUI: C0476273
Disease: Respiratory distress
Respiratory distress
259 0 41 0.15 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 41 0.15 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 41 0.14 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
318 0 41 0.13 0 0
CUI: C0018681
Disease: Headache
Headache
338 0 43 0.13 0 0
CUI: C4022989
Disease: Absent outer dynein arms
Absent outer dynein arms
6 0 6 0.12 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility
9 0 6 0.12 0 0
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media
120 0 17 0.11 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 7 1.0E-01 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 7 1.0E-01 0 0
CUI: C4022986
Disease: Absent inner and outer dynein arms
Absent inner and outer dynein arms
7 0 5 1.0E-01 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
30 0 7 9.9E-02 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 7 9.9E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 7 9.9E-02 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly
410 0 41 9.8E-02 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding)
427 0 41 9.4E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
39 0 7 8.7E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 7 8.7E-02 0 0
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps
484 0 42 8.6E-02 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
473 0 41 8.5E-02 0 0