EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
    5.3.1.8 | mannose-6-phosphate isomerase deficiency |
9535779 |
A novel disorder of N-glycosylation due to phosphomannose isomerase deficiency. |
causal interaction
unassigned |
4
0 |
| 5.3.1.8 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
29531722 |
A novel homozygous mutation in the mannose phosphate isomerase gene causing congenital disorder of glycation and hyperinsulinemic hypoglycemia in an infant. |
causal interaction
unassigned |
3
0 |
| 5.3.1.8 | Hypoglycemia |
29531722 |
A novel homozygous mutation in the mannose phosphate isomerase gene causing congenital disorder of glycation and hyperinsulinemic hypoglycemia in an infant. |
causal interaction
unassigned |
3
0 |
| 5.3.1.8 | Congenital Disorders of Glycosylation |
26430078 |
A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase Deficiencies. |
unassigned |
0 |
| 5.3.1.8 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
26430078 |
A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase Deficiencies. |
unassigned |
0 |
| 5.3.1.8 | mannose-6-phosphate isomerase deficiency |
26430078 |
A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase Deficiencies. |
unassigned |
0 |
| 5.3.1.8 | Congenital Disorders of Glycosylation |
22899857 |
A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation. |
unassigned |
0 |
| 5.3.1.8 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
22899857 |
A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation. |
unassigned |
0 |
| 5.3.1.8 | mannose-6-phosphate isomerase deficiency |
22899857 |
A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation. |
unassigned |
0 |
| 5.3.1.8 | Alcohol Withdrawal Delirium |
5573906 |
Activity of aldolase, aminotransferases, phosphohexoisomerase and ceruloplasmin in the course of delirium tremens. |
unassigned |
0 |
