Pathways Knowlegdes

Biological pathway database

Pathway DOIs Note
Biosynthesis of aldosterone and cortisol

Accession ID: WikiPathways:WP508		 -
Steroid hormone precursor biosynthesis

Accession ID: WikiPathways:WP5277
  • 10.1016/j.jsbmb.2019.105439
 Schiffer L, Barnard L, Baranowski ES, Gilligan LC, Taylor AE, Arlt W, Shackleton CHL, Storbeck K. Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: A comprehensive review. The Journal of Steroid Biochemistry and Molecular Biology. 2019 Nov;194():105439. doi: 10.1016/j.jsbmb.2019.105439.
Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH

Accession ID: PathBank:SMP0120690		 -
11-beta-Hydroxylase Deficiency (CYP11B1)

Accession ID: PathBank:SMP0120858		 -
Corticosterone Methyl Oxidase I Deficiency (CMO I)

Accession ID: PathBank:SMP0120641		 -
Apparent Mineralocorticoid Excess Syndrome

Accession ID: PathBank:SMP0120649		 -
Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Accession ID: PathBank:SMP0000373		 -
21-Hydroxylase Deficiency (CYP21)

Accession ID: PathBank:SMP0000576		 -
3-beta-Hydroxysteroid Dehydrogenase Deficiency

Accession ID: PathBank:SMP0000718		 -
Steroidogenesis

Accession ID: PathBank:SMP0087238		 -
17-alpha-Hydroxylase Deficiency (CYP17)

Accession ID: PathBank:SMP0120849		 -
Corticosterone Methyl Oxidase II Deficiency (CMO II)

Accession ID: PathBank:SMP0120861		 -
3-beta-Hydroxysteroid Dehydrogenase Deficiency

Accession ID: PathBank:SMP0120869		 -
Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120451		 -
21-Hydroxylase Deficiency (CYP21)

Accession ID: PathBank:SMP0120640		 -
11-beta-Hydroxylase Deficiency (CYP11B1)

Accession ID: PathBank:SMP0000575		 -
Apparent Mineralocorticoid Excess Syndrome

Accession ID: PathBank:SMP0000717		 -
Steroidogenesis

Accession ID: PathBank:SMP0063672		 -
Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120672		 -
Corticosterone Methyl Oxidase I Deficiency (CMO I)

Accession ID: PathBank:SMP0120860		 -