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Results 1 - 10 of 27 > >>
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Hyperoxaluria, Primary
4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition.
causal interaction
diagnostic usage
ongoing research
therapeutic application
1
2
1
1
Hyperoxaluria, Primary
Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3.
causal interaction
unassigned
4
0
Hyperoxaluria, Primary
Dihydrodipicolinate Synthase: Structure, Dynamics, Function, and Evolution.
therapeutic application
unassigned
3
0
Hyperoxaluria, Primary
Folding Defects Leading to Primary Hyperoxaluria.
ongoing research
therapeutic application
unassigned
1
1
0
Hyperoxaluria, Primary
HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.
causal interaction
diagnostic usage
unassigned
4
1
0
Hyperoxaluria, Primary
Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3.
causal interaction
unassigned
4
0
Hyperoxaluria, Primary
Mutation Hot Spot Region in the HOGA1 Gene Associated with Primary Hyperoxaluria Type 3 in the Chinese Population.
unassigned
0
Hyperoxaluria, Primary
Mutations in DHDPSL are responsible for primary hyperoxaluria type III.
causal interaction
diagnostic usage
unassigned
4
1
0
Hyperoxaluria, Primary
Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children.
causal interaction
ongoing research
therapeutic application
unassigned
2
2
1
0
4-hydroxy-2-oxoglutarate aldolase deficiency
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies.
causal interaction
therapeutic application
unassigned
4
3
0
Results 1 - 10 of 27 > >>