EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.14.14.32 | 11beta-hydroxysteroid dehydrogenase (nad+) deficiency |
18407194 |
Renin-Independent hypermineralocorticoidism. |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 1.14.14.32 | 11beta-hydroxysteroid dehydrogenase deficiency |
10915016 |
Epidemiologic study of adrenal gland disorders in Japan. |
causal interaction
unassigned |
3
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
174842 |
Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency. |
unassigned |
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
308800 |
Hypertension due to 17alpha-hydroxylase deficiency. |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
610421 |
A case of 17alpha-hydroxylase deficiency with symptoms mimicking testicular feminization. |
causal interaction
unassigned |
4
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
663934 |
Simultaneous determination of plasma 11-deoxycorticosterone, 18-hydroxy-11-deoxycorticosterone, and aldosterone in man. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
973620 |
Hypokalemic crisis simulating intestinal obstruction in a 4-year-old girl. A consequence of 17alpha-hydroxylase deficiency. |
causal interaction
unassigned |
3
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
8943512 |
Ovarian hyperstimulation syndrome with low oestradiol in non-classical 17 alpha-hydroxylase, 17,20-lyase deficiency: what is the role of oestrogens? |
causal interaction
unassigned |
4
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
9029728 |
The regulation of 17,20 lyase activity. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
3
1
0 |
| 1.14.14.32 | 17alpha-hydroxyprogesterone deacetylase deficiency |
9177409 |
A 5'-splice site mutation in the cytochrome P450 steroid 17alpha-hydroxylase gene in 17alpha-hydroxylase deficiency. |
causal interaction
unassigned |
4
0 |
