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Results 1 - 10 of 92 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.13beta-hydroxy-delta5-steroid dehydrogenase deficiency 18252794 Carboxyl-Terminal Mutations in 3{beta}-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia. causal interaction
diagnostic usage
therapeutic application
unassigned
4
3
1
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Addison Disease 12137862 Steroid-cell autoantibodies are preferentially expressed in women with premature ovarian failure who have adrenal autoimmunity. causal interaction
diagnostic usage
ongoing research
therapeutic application
2
3
2
1
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adenoma 9625451 Immunohistochemical study of cytochrome b5 in human adrenal gland and in adrenocortical adenomas from patients with Cushing's syndrome. causal interaction
diagnostic usage
therapeutic application
unassigned
3
3
1
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 10599696 New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes. causal interaction
ongoing research
unassigned
4
2
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 11196452 A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency. causal interaction
unassigned
4
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 12050213 A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. causal interaction
ongoing research
unassigned
4
2
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 12050224 Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency. causal interaction
diagnostic usage
therapeutic application
unassigned
4
3
1
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 12428206 Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase deficiency. causal interaction
unassigned
4
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenal Hyperplasia, Congenital 15632317 Molecular biology of the 3beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family. causal interaction
unassigned
4
0
Show all pathways known for 5.3.3.1Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.1Adrenocortical Hyperfunction 15080470 Trilostane treatment in dogs with pituitary-dependent hyperadrenocorticism. diagnostic usage
therapeutic application
unassigned
2
1
0
Results 1 - 10 of 92 > >>