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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
The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3.
causal interaction
diagnostic usage
ongoing research
unassigned
4
4
2
0
Hyperoxaluria, Primary
The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III.
causal interaction
diagnostic usage
ongoing research
unassigned
1
4
2
0
Hyperoxaluria, Primary
Re: Mutations in DHDPSL are Responsible for Primary Hyperoxaluria Type III.
causal interaction
diagnostic usage
therapeutic application
unassigned
4
1
1
0
4-hydroxy-2-oxoglutarate aldolase deficiency
Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism.
causal interaction
diagnostic usage
unassigned
4
1
0
Hyperoxaluria, Primary
Mutations in DHDPSL are responsible for primary hyperoxaluria type III.
causal interaction
diagnostic usage
unassigned
4
1
0
Hyperoxaluria, Primary
Primary hyperoxaluria type III-a model for studying perturbations in glyoxylate metabolism.
causal interaction
diagnostic usage
unassigned
4
1
0
Hyperoxaluria, Primary
Two Novel HOGA1 Splicing Mutations Identified in a Chinese Patient with Primary Hyperoxaluria Type 3.
causal interaction
diagnostic usage
unassigned
3
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
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
Results 1 - 10 of 27 > >>