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: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 9.7E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 9.7E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 9.7E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 9.7E-03 0 0
CUI: C0026684
Disease: Mucocele of appendix
Mucocele of appendix 		1 0 1 9.7E-03 0 0
CUI: C0029163
Disease: Oral Hemorrhage
Oral Hemorrhage 		1 0 1 9.7E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 9.7E-03 0 0
CUI: C0035468
Disease: Rhinoscleroma
Rhinoscleroma 		1 0 1 9.7E-03 0 0
CUI: C0042392
Disease: Vasitis
Vasitis 		1 0 1 9.7E-03 0 0
CUI: C0151686
Disease: Growth retardation
Growth retardation 		1 0 1 9.7E-03 0 0
CUI: C0153572
Disease: Malignant Placental Neoplasm
Malignant Placental Neoplasm 		1 0 1 9.7E-03 0 0
CUI: C0154157
Disease: Postoperative hypothyroidism
Postoperative hypothyroidism 		1 0 1 9.7E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 9.7E-03 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis 		1 0 1 9.7E-03 0 0
CUI: C0220761
Disease: Dizygotic twins (disorder)
Dizygotic twins (disorder) 		1 0 1 9.7E-03 0 0
CUI: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome 		1 0 1 9.7E-03 0 0
CUI: C0232694
Disease: Hyperactive bowel sounds
Hyperactive bowel sounds 		1 0 1 9.7E-03 0 0
CUI: C0233200
Disease: Cullen's sign
Cullen's sign 		1 0 1 9.7E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 9.7E-03 0 0
CUI: C0236124
Disease: Gastrointestinal obstruction
Gastrointestinal obstruction 		1 0 1 9.7E-03 0 0
CUI: C0238185
Disease: Juvenile myxedema
Juvenile myxedema 		1 0 1 9.7E-03 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 9.7E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 9.7E-03 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 9.7E-03 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 9.7E-03 0 0