EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.14.16.1 | 4a-hydroxytetrahydrobiopterin dehydratase deficiency |
1405480 |
Suspected pterin-4a-carbinolamine dehydratase deficiency: hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin. |
causal interaction
unassigned |
3
0 |
| 1.14.16.1 | 6,7-dihydropteridine reductase deficiency |
571268 |
[Comparative effects of different inhibitors of phenylalanine hydroxylase and dihydropteridine reductase. In vivo and in vitro study in rats] |
causal interaction
unassigned |
3
0 |
| 1.14.16.1 | 6,7-dihydropteridine reductase deficiency |
7452296 |
Neopterin and biopterin levels in patients with atypical forms of phenylketonuria. |
causal interaction
unassigned |
4
0 |
| 1.14.16.1 | 6-pyruvoyltetrahydropterin synthase deficiency |
21933604 |
Phenylketonuria in Hong Kong Chinese: a call for hyperphenylalaninemia newborn screening in the Special Administrative Region, China. |
causal interaction
unassigned |
3
0 |
| 1.14.16.1 | Acquired Immunodeficiency Syndrome |
10980574 |
Structural interpretation of mutations in phenylalanine hydroxylase protein aids in identifying genotype-phenotype correlations in phenylketonuria. |
causal interaction
unassigned |
4
0 |
| 1.14.16.1 | Acquired Immunodeficiency Syndrome |
26458252 |
Discovery of a Specific Inhibitor of Pyomelanin Synthesis in Legionella pneumophila. |
causal interaction
unassigned |
1
0 |
| 1.14.16.1 | acyl-coa dehydrogenase deficiency |
30904546 |
Expanded newborn screening for inherited metabolic disorders and genetic characteristics in a southern Chinese population. |
causal interaction
unassigned |
4
0 |
| 1.14.16.1 | Amyotrophic Lateral Sclerosis |
30037610 |
Phenylalanine hydroxylase: A biomarker of disease susceptibility in Parkinson's disease and Amyotrophic lateral sclerosis. |
causal interaction
unassigned |
3
0 |
| 1.14.16.1 | Amyotrophic Lateral Sclerosis |
30939113 |
Drug S-oxidation and phenylalanine hydroxylase: a biomarker for neurodegenerative susceptibility in Parkinson's disease and amyotrophic lateral sclerosis. |
causal interaction
therapeutic application
unassigned |
3
2
0 |
| 1.14.16.1 | Anemia, Sickle Cell |
32010984 |
Maternal genetic disorders and fetal development. |
causal interaction
unassigned |
4
0 |
