EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.13.11.5 | Alkaptonuria |
1401313 |
Alkaptonuria and ochronosis: case report and review. |
causal interaction unassigned |
3 0 |
1.13.11.5 | Alkaptonuria |
1813514 |
Ocular ochronosis from alkaptonuria. |
causal interaction unassigned |
4 0 |
1.13.11.5 | Alkaptonuria |
2686878 |
Ochronosis: a report of a case and a review of literature. |
unassigned |
0 |
1.13.11.5 | Alkaptonuria |
3180550 |
Alkaptonuria and ochronosis in three siblings. Ascorbic acid treatment monitored by urinary HGA excretion. |
ongoing research unassigned |
1 0 |
1.13.11.5 | Alkaptonuria |
3375493 |
[Ochronotic arthropathy in alkaptonuria. Radiological manifestations and physiopathological signs] |
causal interaction unassigned |
4 0 |
1.13.11.5 | Alkaptonuria |
6543841 |
Neonatal severe primary hyperparathyroidism and alkaptonuria in a boy born to related parents with familial hypocalciuric hypercalcemia. |
unassigned |
0 |
1.13.11.5 | Alkaptonuria |
7568087 |
Fungal metabolic model for human type I hereditary tyrosinaemia. |
causal interaction diagnostic usage therapeutic application unassigned |
4 3 4 0 |
1.13.11.5 | Alkaptonuria |
8782815 |
The molecular basis of alkaptonuria. |
causal interaction unassigned |
3 0 |
1.13.11.5 | Alkaptonuria |
9069115 |
Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse. |
therapeutic application unassigned |
1 0 |
1.13.11.5 | Alkaptonuria |
9154114 |
Molecular defects in alkaptonuria. |
diagnostic usage unassigned |
2 0 |