Pathways Knowlegdes

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Pathway DOIs Note
Biochemical pathways: part I

Accession ID: WikiPathways:WP3604
  • 10.1016/s0303-2647(98)00019-7
 Michal G. On representation of metabolic pathways. Biosystems. 1998 Jun;47(1-2):1–7. doi: 10.1016/s0303-2647(98)00019-7. PMID: 9715748.
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		 -
Apparent Mineralocorticoid Excess Syndrome

Accession ID: PathBank:SMP0120868		 -