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: C0220994
Disease: Hyperammonemia
Hyperammonemia
102 0 33 0.22 0 0
CUI: C0023380
Disease: Lethargy
Lethargy
160 0 42 0.21 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria
26 0 17 0.20 0 0
CUI: C0022638
Disease: Ketosis
Ketosis
119 0 28 0.17 0 0
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema
26 0 13 0.14 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia
15 0 11 0.13 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 45 0.13 0 0
Transient neonatal diabetes mellitus
23 0 11 0.12 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
42 0 13 0.12 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria
53 0 14 0.12 0 0
CUI: C0151747
Disease: Renal tubular disorder
Renal tubular disorder
64 0 15 0.12 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness
31 0 11 0.11 0 0
Contractures of the joints of the lower limbs
12 0 9 0.11 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 16 0.11 0 0
CUI: C0003635
Disease: Apraxias
Apraxias
71 0 14 0.10 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas
20 0 9 0.10 0 0
DIABETES MELLITUS, PERMANENT NEONATAL
20 0 9 0.10 0 0
Neonatal insulin-dependent diabetes mellitus
10 0 8 1.0E-01 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 8 9.5E-02 0 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge
39 0 10 9.3E-02 0 0
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia
52 0 11 9.2E-02 0 0
CUI: C1306587
Disease: Acute encephalopathy
Acute encephalopathy
31 0 9 9.0E-02 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells
7 0 7 9.0E-02 0 0
CUI: C2830004
Disease: Somnolence
Somnolence
87 0 13 8.6E-02 0 0
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
62 0 11 8.5E-02 0 0