EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.14.15.4 | 3(or 17)beta-hydroxysteroid dehydrogenase deficiency |
9536212 |
Congenital adrenal hyperplasia. |
causal interaction
unassigned |
4
0 |
| 1.14.15.4 | 3(or 17)beta-hydroxysteroid dehydrogenase deficiency |
9880115 |
Congenital adrenal hyperplasia in pregnancy. |
causal interaction
unassigned |
4
0 |
| 1.14.15.4 | 3beta-hydroxy-delta5-steroid dehydrogenase deficiency |
30811025 |
Comprehensive genotyping of Turkish women with hirsutism. |
causal interaction
unassigned |
2
0 |
| 1.14.15.4 | 46, XX Disorders of Sex Development |
13890647 |
[A case of female pseudohermaphroditism caused by adrenal deficiency in 21-hydroxylase and 11-hydroxylase.] |
causal interaction
unassigned |
4
0 |
| 1.14.15.4 | Acidosis |
7758082 |
[The human genome--chromosome 8] |
causal interaction
unassigned |
1
0 |
| 1.14.15.4 | Acidosis, Renal Tubular |
7758082 |
[The human genome--chromosome 8] |
causal interaction
unassigned |
1
0 |
| 1.14.15.4 | Acne Vulgaris |
16670167 |
Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 1.14.15.4 | Acne Vulgaris |
16895568 |
[Acne infantum as presenting symptom of congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency] |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 1.14.15.4 | Acne Vulgaris |
28713602 |
Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 1.14.15.4 | Acromegaly |
17003099 |
CYP11B2 -344T/C gene polymorphism and blood pressure in patients with acromegaly. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
2
2 |
