EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.5.1.8 | Cystinuria |
571908 |
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria. |
causal interaction therapeutic application unassigned |
1 1 0 |
1.5.1.8 | Hyperlysinemias |
463877 |
Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology. |
causal interaction unassigned |
3 0 |
1.5.1.8 | Hyperlysinemias |
571908 |
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria. |
causal interaction therapeutic application unassigned |
1 1 0 |
1.5.1.8 | Hyperlysinemias |
934735 |
Multiple enzyme defects in familial hyperlysinemia. |
causal interaction unassigned |
4 0 |
1.5.1.8 | Hyperlysinemias |
5796356 |
Familial hyperlysinemia with lysine-ketoglutarate reductase insufficiency. |
causal interaction unassigned |
3 0 |
1.5.1.8 | Hyperlysinemias |
6407303 |
The prognosis of hyperlysinemia: an interim report. |
causal interaction diagnostic usage unassigned |
3 3 0 |
1.5.1.8 | Hyperlysinemias |
6434529 |
Familial hyperlysinemias. Purification and characterization of the bifunctional aminoadipic semialdehyde synthase with lysine-ketoglutarate reductase and saccharopine dehydrogenase activities. |
causal interaction ongoing research therapeutic application unassigned |
4 1 1 0 |
1.5.1.8 | Infections |
19374926 |
Proteomic analysis of fungal host factors differentially expressed by Fusarium graminearum infected with Fusarium graminearum virus-DK21. |
causal interaction unassigned |
4 0 |
1.5.1.8 | saccharopine dehydrogenase (nadp+, l-lysine-forming) deficiency |
571908 |
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria. |
causal interaction therapeutic application unassigned |
1 1 0 |
1.5.1.8 | saccharopine dehydrogenase (nadp+, l-lysine-forming) deficiency |
934735 |
Multiple enzyme defects in familial hyperlysinemia. |
causal interaction unassigned |
4 0 |