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: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis 		1 0 1 2.0E-02 0 0
CUI: C0017128
Disease: Gastric Fistula
Gastric Fistula 		1 0 1 2.0E-02 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 2.0E-02 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 2.0E-02 0 0
CUI: C0152074
Disease: Ethiopian cutaneous leishmaniasis
Ethiopian cutaneous leishmaniasis 		1 0 1 2.0E-02 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 2.0E-02 0 0
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		1 0 1 2.0E-02 0 0
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism 		1 0 1 2.0E-02 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 2.0E-02 0 0
CUI: C0266062
Disease: Posterior open bite
Posterior open bite 		1 0 1 2.0E-02 0 0
CUI: C0267066
Disease: Chalasia of lower esophageal sphincter
Chalasia of lower esophageal sphincter 		1 0 1 2.0E-02 0 0
CUI: C0268309
Disease: Inherited disorder of bilirubin metabolism
Inherited disorder of bilirubin metabolism 		1 0 1 2.0E-02 0 0
CUI: C0268417
Disease: Pancreatic trypsinogen deficiency
Pancreatic trypsinogen deficiency 		1 0 1 2.0E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy 		1 0 1 2.0E-02 0 0
CUI: C0271271
Disease: Xerotic keratitis
Xerotic keratitis 		1 0 1 2.0E-02 0 0
CUI: C0271662
Disease: Gestational diabetes mellitus, class A>1<
Gestational diabetes mellitus, class A>1< 		1 0 1 2.0E-02 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction 		1 0 1 2.0E-02 0 0
CUI: C0338329
Disease: recurrent childhood brain stem glioma
recurrent childhood brain stem glioma 		1 0 1 2.0E-02 0 0
CUI: C0339882
Disease: Laryngeal amyloidosis
Laryngeal amyloidosis 		1 0 1 2.0E-02 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome 		1 0 1 2.0E-02 0 0
CUI: C0341702
Disease: Acquired Fanconi syndrome
Acquired Fanconi syndrome 		1 0 1 2.0E-02 0 0
CUI: C0342735
Disease: Cytosolic acetoacetyl-CoA thiolase deficiency
Cytosolic acetoacetyl-CoA thiolase deficiency 		1 0 1 2.0E-02 0 0
CUI: C0342890
Disease: Primary combined hyperlipidemia
Primary combined hyperlipidemia 		1 0 1 2.0E-02 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 2.0E-02 0 0
CUI: C0344882
Disease: Tetralogy of Fallot with pulmonary atresia
Tetralogy of Fallot with pulmonary atresia 		1 0 1 2.0E-02 0 0