EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.14.15.5 | Adrenogenital Syndrome |
16426683 |
CYP17- and CYP11B-dependent steroid hydroxylases as drug development targets. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 1.14.15.5 | cholinesterase deficiency |
20733503 |
Genetic screening in the Persian Jewish community: A pilot study. |
causal interaction
unassigned |
4
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
3510001 |
Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency. |
causal interaction
unassigned |
4
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
6277129 |
The effect of ACTH stimulation on plasma steroids in two patients with congenital hypoaldosteronism and in their relatives. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
7745009 |
Multisteroid analysis in children with terminal aldosterone biosynthesis defects. |
causal interaction
unassigned |
4
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
8929880 |
Congenital hypoaldosteronism: the Visser-Cost syndrome revisited. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
9360501 |
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
9625333 |
Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II. |
causal interaction
unassigned |
4
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
22931312 |
Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 1.14.15.5 | corticosterone 18-monooxygenase deficiency |
25102047 |
Computational analysis of functional single nucleotide polymorphisms associated with the CYP11B2 gene. |
causal interaction
unassigned |
4
0 |
