Steroid inherited metabolic disorder
MONDO:0005523Errors in metabolic processing of steroids resulting from inborn genetic mutations that are inherited or acquired in utero.
39 clinical trials for this condition and its sub-types, 0 tagged with Steroid inherited metabolic disorder itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Steroid inherited metabolic disorder
-
Congenital adrenal hyperplasia 36 trials · 38 incl. sub-types
8 sub-types
- Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 20 trials Sub-types →
- Classic congenital adrenal hyperplasia 5 trials
- Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 1 trial
- Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency 1 trial
- Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency 1 trial
- Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency 1 trial
- Congenital lipoid adrenal hyperplasia due to STAR deficency 1 trial Sub-types →
- Non-classic congenital adrenal hyperplasia 0 trials
-
Congenital bile acid synthesis defect 1 trial · 2 incl. sub-types
6 sub-types
Most studied deeper sub-types
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form
(0)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form
(0)
Classic congenital lipoid adrenal hyperplasia due to STAR deficency
(0)
Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.