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: C0149516
Disease: Chronic sinusitis
Chronic sinusitis 		205 0 42 0.17 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 18 0.17 0 0
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		13 0 13 0.16 0 0
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		13 0 13 0.16 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 36 43 0.14 2 5.1E-02
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 43 0.13 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections 		318 0 45 0.13 0 0
CUI: C3552099
Disease: Respiratory insufficiency due to defective ciliary clearance
Respiratory insufficiency due to defective ciliary clearance 		10 0 10 0.12 0 0
CUI: C0018681
Disease: Headache
Headache 		338 75 44 0.12 2 2.6E-02
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis 		15 0 9 0.10 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		473 0 51 0.10 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 43 9.6E-02 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 10 9.3E-02 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 43 9.2E-02 0 0
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media 		120 0 17 9.2E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 9 8.8E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 9 8.8E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 9 8.7E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 9 8.7E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 9 8.7E-02 0 0
CUI: C1855675
Disease: Arima syndrome
Arima syndrome 		11 0 7 8.1E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 9 8.0E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 9 8.0E-02 0 0
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		484 0 42 8.0E-02 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 8 8.0E-02 0 0