Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism

Pathway network for the Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism SuperPath

Sources:
  • WikiPathways
  • PubChem
  • Reactome

Pathways in the Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism SuperPath

Gene overlap in member pathways for Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Steroid inherited metabolic disorderDirect
2Lipoid congenital adrenal hyperplasiaEnrichmentCYP11A1, HSD3B2, POR8.06
3Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiencyEnrichmentHSD3B23.53
4Hypospadias 1, x-linkedEnrichmentHSD3B23.53
53 beta-hydroxysteroid dehydrogenase deficiencyEnrichmentHSD3B23.53
6Adrenal insufficiency, congenital, with 46,xy sex reversal, partial or completeEnrichmentCYP11A13.43
7Brachycephaly, deafness, cataract, microstomia, and impaired intellectual developmentEnrichmentPOR3.43
8Inherited isolated adrenal insufficiency due to partial cyp11a1 deficiencyEnrichmentCYP11A13.43
9Corticosterone methyloxidase type i deficiencyEnrichmentCYP11B23.13
10Antley-bixler syndrome with genital anomalies and disordered steroidogenesisEnrichmentPOR3.13
11Corticosterone methyloxidase type ii deficiencyEnrichmentCYP11B23.13
12Antley-bixler syndrome without genital anomalies or disordered steroidogenesisEnrichmentPOR3.13
13Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiencyEnrichmentPOR3.13
14Cytochrome p450 oxidoreductase deficiencyEnrichmentPOR3.13
15Familial hypoaldosteronismEnrichmentCYP11B23.13
16Early-onset familial hypoaldosteronismEnrichmentCYP11B23.13
17Hyperaldosteronism, familial, type iEnrichmentCYP11B22.66
18Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyEnrichmentCYP11A12.66
1921-hydroxylase-deficient congenital adrenal hyperplasiaEnrichmentCYP11A12.66
20Primary ovarian insufficiencyEnrichmentPOR1.67

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