Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Accession ID: PathBank:SMP0000373 |
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| 21-Hydroxylase Deficiency (CYP21) Accession ID: PathBank:SMP0000576 |
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| 3-beta-Hydroxysteroid Dehydrogenase Deficiency Accession ID: PathBank:SMP0000718 |
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| Steroidogenesis Accession ID: PathBank:SMP0087238 |
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| 17-alpha-Hydroxylase Deficiency (CYP17) Accession ID: PathBank:SMP0120849 |
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| Corticosterone Methyl Oxidase II Deficiency (CMO II) Accession ID: PathBank:SMP0120861 |
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| 3-beta-Hydroxysteroid Dehydrogenase Deficiency Accession ID: PathBank:SMP0120869 |
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| Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency Accession ID: PathBank:SMP0120451 |
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| 21-Hydroxylase Deficiency (CYP21) Accession ID: PathBank:SMP0120640 |
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| 11-beta-Hydroxylase Deficiency (CYP11B1) Accession ID: PathBank:SMP0000575 |
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| Apparent Mineralocorticoid Excess Syndrome Accession ID: PathBank:SMP0000717 |
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| Steroidogenesis Accession ID: PathBank:SMP0063672 |
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| Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency Accession ID: PathBank:SMP0120672 |
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| Corticosterone Methyl Oxidase I Deficiency (CMO I) Accession ID: PathBank:SMP0120860 |
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| Apparent Mineralocorticoid Excess Syndrome Accession ID: PathBank:SMP0120868 |
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| 17-alpha-Hydroxylase Deficiency (CYP17) Accession ID: PathBank:SMP0120630 |
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| Corticosterone Methyl Oxidase II Deficiency (CMO II) Accession ID: PathBank:SMP0120642 |
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| 3-beta-Hydroxysteroid Dehydrogenase Deficiency Accession ID: PathBank:SMP0120650 |
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| Steroidogenesis Accession ID: PathBank:SMP0000130 |
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| Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH Accession ID: PathBank:SMP0000371 |
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