EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.14.15.6 | 3(or 17)beta-hydroxysteroid dehydrogenase deficiency |
1879398 |
17 alpha-hydroxylation deficiency. |
causal interaction unassigned |
4 0 |
1.14.15.6 | 3(or 17)beta-hydroxysteroid dehydrogenase deficiency |
7810070 |
Genetic diseases of steroid metabolism. |
causal interaction unassigned |
4 0 |
1.14.15.6 | 3beta-hydroxy-delta5-steroid dehydrogenase deficiency |
24793988 |
Steroidogenesis of the testis -- new genes and pathways. |
causal interaction unassigned |
4 0 |
1.14.15.6 | Abortion, Spontaneous |
10418987 |
Molecular pathology and mechanism of action of the steroidogenic acute regulatory protein, StAR. |
causal interaction unassigned |
2 0 |
1.14.15.6 | Abortion, Spontaneous |
30044146 |
Association between LRH-1 single nucleotide polymorphisms and unexplained recurrent spontaneous abortion in Chinese Han couples. |
unassigned |
0 |
1.14.15.6 | Addison Disease |
7916911 |
Characterization of adrenal autoantigens recognized by sera from patients with autoimmune polyglandular syndrome (APS) type I. |
unassigned |
0 |
1.14.15.6 | Addison Disease |
8106620 |
Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease. |
diagnostic usage ongoing research therapeutic application unassigned |
3 4 1 0 |
1.14.15.6 | Addison Disease |
8626850 |
Autoantibodies to steroidogenic enzymes in autoimmune polyglandular syndrome, Addison's disease, and premature ovarian failure. |
causal interaction diagnostic usage ongoing research unassigned |
1 4 1 0 |
1.14.15.6 | Addison Disease |
12092456 |
Autoantibodies in autoimmune polyendocrine syndrome type II. |
causal interaction diagnostic usage unassigned |
4 4 0 |
1.14.15.6 | Addison Disease |
15747502 |
Autoantibodies against CYP2D6 and other drug-metabolizing enzymes in autoimmune hepatitis type 2. |
causal interaction therapeutic application unassigned |
3 2 0 |