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: C1306587
Disease: Acute encephalopathy
Acute encephalopathy 		0 3 0 0 1 6.7E-02
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 9.1E-03 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 9.1E-03 0 0
CUI: C0031946
Disease: Pinta
Pinta 		1 0 1 9.1E-03 0 0
CUI: C0033132
Disease: Cerebellar Degenerations, Primary
Cerebellar Degenerations, Primary 		1 0 1 9.1E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 9.1E-03 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 9.1E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 9.1E-03 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 9.1E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 9.1E-03 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 9.1E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 9.1E-03 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 9.1E-03 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis 		1 0 1 9.1E-03 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 9.1E-03 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 9.1E-03 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 9.1E-03 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 9.1E-03 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 9.1E-03 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 9.1E-03 0 0
CUI: C0270755
Disease: Corticostriatal-Spinal Degeneration
Corticostriatal-Spinal Degeneration 		1 0 1 9.1E-03 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 9.1E-03 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 9.1E-03 0 0
CUI: C0311364
Disease: Anemia due to decreased red cell production
Anemia due to decreased red cell production 		1 0 1 9.1E-03 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 9.1E-03 0 0