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: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
166 122 81 0.49 4 3.3E-02
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 10 81 9.6E-02 4 0.40
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
109 0 11 6.1E-02 0 0
CUI: C0240783
Disease: Increased circulating renin level
Increased circulating renin level
10 0 5 5.8E-02 0 0
Mitochondrial Respiratory Chain Deficiencies
49 0 7 5.7E-02 0 0
CUI: C0268435
Disease: Renal Tubular Acidosis, Type II
Renal Tubular Acidosis, Type II
13 0 5 5.6E-02 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder
93 0 9 5.5E-02 0 0
CUI: C0033805
Disease: Pseudohypoaldosteronism
Pseudohypoaldosteronism
19 0 5 5.3E-02 0 0
Congenital glucose-galactose malabsorption
19 0 5 5.3E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 9 5.1E-02 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
22 0 5 5.1E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 8 5.1E-02 0 0
CUI: C0029438
Disease: Massive Osteolyses
Massive Osteolyses
44 0 6 5.0E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 6 4.7E-02 0 0
Hyperactive renin-angiotensin system
8 0 4 4.7E-02 0 0
CUI: C1257958
Disease: Glucose Metabolism Disorders
Glucose Metabolism Disorders
32 0 5 4.6E-02 0 0
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I
36 0 5 4.5E-02 0 0
Refractory anemia with ringed sideroblasts
36 0 5 4.5E-02 0 0
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism
84 0 7 4.4E-02 0 0
CUI: C0878787
Disease: Growth failure
Growth failure
84 0 7 4.4E-02 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia
61 0 6 4.4E-02 0 0
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea
62 0 6 4.4E-02 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 16 4.3E-02 0 0
CUI: C0080218
Disease: Tethered Cord Syndrome
Tethered Cord Syndrome
41 0 5 4.3E-02 0 0
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase
17 0 4 4.3E-02 0 0