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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 6.8E-03 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 6.8E-03 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 6.8E-03 0 0
CUI: C0011548
Disease: Dependent Personality Disorder
Dependent Personality Disorder 		1 0 1 6.8E-03 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced 		1 0 1 6.8E-03 0 0
CUI: C0022580
Disease: Punctate keratosis
Punctate keratosis 		1 0 1 6.8E-03 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 6.8E-03 0 0
CUI: C0029291
Disease: Psittacosis
Psittacosis 		1 0 1 6.8E-03 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 6.8E-03 0 0
CUI: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 6.8E-03 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis 		1 0 1 6.8E-03 0 0
CUI: C0041651
Disease: Uncomplicated alcohol withdrawal
Uncomplicated alcohol withdrawal 		1 0 1 6.8E-03 0 0
CUI: C0079037
Disease: Branchial Clefts-Congenital disorder
Branchial Clefts-Congenital disorder 		1 0 1 6.8E-03 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis 		1 0 1 6.8E-03 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 6.8E-03 0 0
CUI: C0151536
Disease: Stenosis of bronchus
Stenosis of bronchus 		1 0 1 6.8E-03 0 0
CUI: C0151686
Disease: Growth retardation
Growth retardation 		1 0 1 6.8E-03 0 0
CUI: C0154628
Disease: Hyperkinetic conduct disorder of childhood
Hyperkinetic conduct disorder of childhood 		1 0 1 6.8E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 6.8E-03 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast 		1 0 1 6.8E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 6.8E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 6.8E-03 0 0
CUI: C0221745
Disease: Depression suicidal
Depression suicidal 		1 0 1 6.8E-03 0 0
CUI: C0221785
Disease: Pain in wrist
Pain in wrist 		1 0 1 6.8E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 6.8E-03 0 0