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: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue 		19 0 15 0.18 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 15 0.18 0 0
CUI: C0149516
Disease: Chronic sinusitis
Chronic sinusitis 		205 0 43 0.18 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 16 0.18 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 18 0.17 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 15 0.16 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: C0010200
Disease: Coughing
Coughing 		235 0 42 0.15 0 0
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 15 0.15 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 17 0.15 0 0
CUI: C0476273
Disease: Respiratory distress
Respiratory distress 		259 0 44 0.15 0 0
CUI: C0040412
Disease: Fissured tongue
Fissured tongue 		36 0 15 0.15 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 15 0.15 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 15 0.15 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease 		38 0 15 0.15 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 16 0.14 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 15 0.14 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		272 36 43 0.14 1 2.4E-02
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst 		60 0 17 0.14 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 15 0.14 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		63 0 17 0.13 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 44 0.13 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 15 0.13 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		53 0 15 0.13 0 0