EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.3.99.5 | 3(or 17)beta-hydroxysteroid dehydrogenase deficiency |
16148681 |
Masculinizing genitoplasty in intersex patients. |
unassigned |
0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
744162 |
Intranuclear binding of [3H]dihydrotestosterone by cultured human fibroblasts. |
causal interaction ongoing research unassigned |
1 1 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
1156691 |
Steroid 5alpha-reductase deficiency in man. An inherited form of male pseudohermaphroditism. |
causal interaction unassigned |
4 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
4432067 |
Steroid 5alpha-reductase deficiency in man: an inherited form of male pseudohermaphroditism. |
causal interaction unassigned |
4 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
10564874 |
New frameshift mutation in the 5alpha-reductase type 2 gene in a Brazilian patient with 5alpha-reductase deficiency. |
causal interaction unassigned |
4 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
10905384 |
Evaluation of the tubular and interstitial functions of the testis in 46,XY patients with ambiguous genitalia. |
causal interaction diagnostic usage unassigned |
4 2 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
10999800 |
Uniparental disomy in steroid 5alpha-reductase 2 deficiency. |
causal interaction unassigned |
3 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
11238515 |
Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability. |
causal interaction unassigned |
4 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
11257695 |
Etiological studies of severe or familial hypospadias. |
diagnostic usage unassigned |
3 0 |
1.3.99.5 | 3-oxo-5alpha-steroid 4-dehydrogenase (acceptor) deficiency |
11392378 |
Disorders linked to insufficient androgen action in male children. |
causal interaction unassigned |
4 0 |