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: C0149991
Disease: TOXIGENIC E COLI
TOXIGENIC E COLI 		2 0 2 0.18 0 0
CUI: C1268936
Disease: Diarrhea-associated hemolytic uremic syndrome
Diarrhea-associated hemolytic uremic syndrome 		5 0 2 0.14 0 0
CUI: C0152517
Disease: Viral gastroenteritis
Viral gastroenteritis 		15 0 3 0.13 0 0
CUI: C0151594
Disease: Hemorrhagic diarrhea
Hemorrhagic diarrhea 		16 0 3 0.12 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 2 0.12 0 0
CUI: C0151565
Disease: Hemorrhagic colitis
Hemorrhagic colitis 		18 0 3 0.12 0 0
CUI: C0162677
Disease: Caliciviridae Infections
Caliciviridae Infections 		1 0 1 9.1E-02 0 0
CUI: C0343379
Disease: Enterotoxigenic Escherichia coli gastrointestinal tract infection
Enterotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 9.1E-02 0 0
CUI: C0940933
Disease: infection as a complication
infection as a complication 		1 0 1 9.1E-02 0 0
CUI: C1279346
Disease: Cardiomyopathy in Duchenne muscular dystrophy
Cardiomyopathy in Duchenne muscular dystrophy 		1 0 1 9.1E-02 0 0
CUI: C1859408
Disease: BOMBAY PHENOTYPE
BOMBAY PHENOTYPE 		1 0 1 9.1E-02 0 0
CUI: C1859411
Disease: PARA-BOMBAY PHENOTYPE
PARA-BOMBAY PHENOTYPE 		1 0 1 9.1E-02 0 0
CUI: C2674252
Disease: VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1
VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 9.1E-02 0 0
CUI: C4749062
Disease: BOMBAY PHENOTYPE, DIGENIC
BOMBAY PHENOTYPE, DIGENIC 		1 0 1 9.1E-02 0 0
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 8.3E-02 0 0
CUI: C0206044
Disease: Infections, Calicivirus
Infections, Calicivirus 		2 0 1 8.3E-02 0 0
CUI: C0265496
Disease: Tetrasomy X
Tetrasomy X 		2 0 1 8.3E-02 0 0
CUI: C3826291
Disease: Gastroenteritis in children
Gastroenteritis in children 		2 0 1 8.3E-02 0 0
CUI: C0264700
Disease: Acute Inferior Myocardial Infarction
Acute Inferior Myocardial Infarction 		3 0 1 7.7E-02 0 0
CUI: C1856143
Disease: HEMOLYTIC UREMIC SYNDROME, TYPICAL
HEMOLYTIC UREMIC SYNDROME, TYPICAL 		3 0 1 7.7E-02 0 0
CUI: C4288409
Disease: Perforin Deficiency
Perforin Deficiency 		3 0 1 7.7E-02 0 0
CUI: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy 		4 0 1 7.1E-02 0 0
CUI: C0265279
Disease: Kniest dysplasia
Kniest dysplasia 		4 0 1 7.1E-02 0 0
CUI: C2882238
Disease: Nonrheumatic aortic (valve) stenosis
Nonrheumatic aortic (valve) stenosis 		5 0 1 6.7E-02 0 0
CUI: C3553449
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 1B
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B 		5 0 1 6.7E-02 0 0