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 1.9E-02 0 0
CUI: C0035091
Disease: Renal Tubular Transport, Inborn Errors
Renal Tubular Transport, Inborn Errors 		1 0 1 1.9E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 1.9E-02 0 0
CUI: C0149662
Disease: Deformity of toe
Deformity of toe 		1 0 1 1.9E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 1.9E-02 0 0
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		1 0 1 1.9E-02 0 0
CUI: C0221168
Disease: Podagra
Podagra 		1 0 1 1.9E-02 0 0
CUI: C0231912
Disease: Nocturnal cough
Nocturnal cough 		1 0 1 1.9E-02 0 0
CUI: C0232567
Disease: Hypergastrinemia
Hypergastrinemia 		1 0 1 1.9E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 1.9E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.9E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 1.9E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 1.9E-02 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 1.9E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 1.9E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 1.9E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 1.9E-02 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 1.9E-02 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 1.9E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 1.9E-02 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 1.9E-02 0 0
CUI: C0342134
Disease: T>3< thyrotoxicosis
T>3< thyrotoxicosis 		1 0 1 1.9E-02 0 0
CUI: C0342377
Disease: Partial hypopituitarism
Partial hypopituitarism 		1 0 1 1.9E-02 0 0
CUI: C0342890
Disease: Primary combined hyperlipidemia
Primary combined hyperlipidemia 		1 0 1 1.9E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 1.9E-02 0 0