Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Pulmonary embolism with pulmonary infarction
1 1 1 0.33 1 2.6E-02
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis
1 2 1 0.33 2 5.3E-02
CUI: C0332882
Disease: congenital obstruction
congenital obstruction
1 0 1 0.33 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome
1 0 1 0.33 0 0
Distal intestinal obstruction syndrome
1 0 1 0.33 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia
1 0 1 0.33 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions
1 2 1 0.33 2 5.3E-02
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration
1 0 1 0.33 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps
1 0 1 0.33 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection
1 0 1 0.33 0 0
CUI: C1840437
Disease: Isolated hyperchlorhidrosis
Isolated hyperchlorhidrosis
1 0 1 0.33 0 0
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
1 0 1 0.33 0 0
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
1 0 1 0.33 0 0
SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
1 0 1 0.33 0 0
PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO
1 0 1 0.33 0 0
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF
1 0 1 0.33 0 0
CUI: C4546076
Disease: Classical cystic fibrosis
Classical cystic fibrosis
1 3 1 0.33 1 2.5E-02
CUI: C4546077
Disease: Atypical cystic fibrosis
Atypical cystic fibrosis
1 5 1 0.33 2 4.9E-02
CUI: C4546414
Disease: Left renal agenesis
Left renal agenesis
1 0 1 0.33 0 0
CUI: C0151476
Disease: Hypochloremic alkalosis
Hypochloremic alkalosis
2 0 1 0.25 0 0
CUI: C0238074
Disease: Chronic pulmonary heart disease
Chronic pulmonary heart disease
2 1 1 0.25 1 2.6E-02
Exertional rhabdomyolysis (disorder)
2 0 1 0.25 0 0
CUI: C0264222
Disease: Acute upper respiratory infection
Acute upper respiratory infection
2 2 1 0.25 2 5.3E-02
CUI: C0268532
Disease: Deficiency of prolidase
Deficiency of prolidase
2 0 1 0.25 0 0
CUI: C0332909
Disease: Congenital unilateral absence
Congenital unilateral absence
2 0 1 0.25 0 0