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: C0588007
Disease: Moderate depression
Moderate depression 		1 0 1 0.12 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions 		1 0 1 0.12 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration 		1 0 1 0.12 0 0
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular 		1 0 1 0.12 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps 		1 0 1 0.12 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection 		1 0 1 0.12 0 0
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria 		1 0 1 0.12 0 0
CUI: C1854631
Disease: Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 		1 0 1 0.12 0 0
CUI: C1864276
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 17 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 17 (disorder) 		1 0 1 0.12 0 0
CUI: C1865433
Disease: VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF 		1 0 1 0.12 0 0
CUI: C1865553
Disease: HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C2063386
Disease: Left atrial appendage thrombosis
Left atrial appendage thrombosis 		1 0 1 0.12 0 0
CUI: C2902961
Disease: Page kidney
Page kidney 		1 0 1 0.12 0 0
CUI: C4016362
Disease: HYPERPRORENINEMIA, FAMILIAL
HYPERPRORENINEMIA, FAMILIAL 		1 0 1 0.12 0 0
CUI: C4016791
Disease: SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS 		1 0 1 0.12 0 0
CUI: C4016792
Disease: PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO
PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C4017360
Disease: APPARENT MINERALOCORTICOID EXCESS, MILD
APPARENT MINERALOCORTICOID EXCESS, MILD 		1 0 1 0.12 0 0
CUI: C4017631
Disease: BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C4022825
Disease: Abnormal urine sodium concentration
Abnormal urine sodium concentration 		1 0 1 0.12 0 0
CUI: C4023214
Disease: Abnormality of circulating cortisol level
Abnormality of circulating cortisol level 		1 0 1 0.12 0 0
CUI: C4329210
Disease: 11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency
11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency 		1 0 1 0.12 0 0
CUI: C4546076
Disease: Classical cystic fibrosis
Classical cystic fibrosis 		1 0 1 0.12 0 0
CUI: C4546077
Disease: Atypical cystic fibrosis
Atypical cystic fibrosis 		1 0 1 0.12 0 0
CUI: C4546414
Disease: Left renal agenesis
Left renal agenesis 		1 0 1 0.12 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 2 0.12 0 0