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: C0006015
Disease: Bordetella Infections
Bordetella Infections 		1 0 1 4.8E-02 0 0
CUI: C0013505
Disease: Echinococcosis, Pulmonary
Echinococcosis, Pulmonary 		1 0 1 4.8E-02 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 4.8E-02 0 0
CUI: C0263442
Disease: Acne Conglobata
Acne Conglobata 		1 0 1 4.8E-02 0 0
CUI: C0268543
Disease: Hyperammonemia, type III
Hyperammonemia, type III 		1 0 1 4.8E-02 0 0
CUI: C0268889
Disease: Prostatic Obstruction
Prostatic Obstruction 		1 0 1 4.8E-02 0 0
CUI: C0276088
Disease: Escherichia coli septicemia
Escherichia coli septicemia 		1 0 1 4.8E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 4.8E-02 0 0
CUI: C0333419
Disease: Sarcoid type granuloma
Sarcoid type granuloma 		1 0 1 4.8E-02 0 0
CUI: C0341352
Disease: Acute suppurative appendicitis
Acute suppurative appendicitis 		1 0 1 4.8E-02 0 0
CUI: C0409326
Disease: Anterior knee pain
Anterior knee pain 		1 0 1 4.8E-02 0 0
CUI: C0523801
Disease: Ornithine measurement
Ornithine measurement 		1 0 1 4.8E-02 0 0
CUI: C0596344
Disease: clinical anxiety
clinical anxiety 		1 0 1 4.8E-02 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria 		1 0 1 4.8E-02 0 0
CUI: C0600039
Disease: Urinary outflow obstruction
Urinary outflow obstruction 		1 0 1 4.8E-02 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc 		1 0 1 4.8E-02 0 0
CUI: C1167659
Disease: Lower respiratory tract inflammation
Lower respiratory tract inflammation 		1 0 1 4.8E-02 0 0
CUI: C1389289
Disease: BB leprosy
BB leprosy 		1 0 1 4.8E-02 0 0
CUI: C1610066
Disease: Urinary tract inflammation
Urinary tract inflammation 		1 0 1 4.8E-02 0 0
CUI: C1719796
Disease: With-the-rule astigmatism
With-the-rule astigmatism 		1 0 1 4.8E-02 0 0
CUI: C1839455
Disease: Properdin Deficiency, Type II
Properdin Deficiency, Type II 		1 0 1 4.8E-02 0 0
CUI: C1839456
Disease: Properdin Deficiency, Type III
Properdin Deficiency, Type III 		1 0 1 4.8E-02 0 0
CUI: C1839458
Disease: Dysfunctional alternative complement pathway
Dysfunctional alternative complement pathway 		1 0 1 4.8E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 4.8E-02 0 0
CUI: C1970472
Disease: PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED
PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED 		1 0 1 4.8E-02 0 0