Glucocorticoid biosynthesis

No Pathway Network information available for Glucocorticoid biosynthesis

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

Disorders associated with Glucocorticoid biosynthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
146,xy sex reversal 8EnrichmentAKR1C2, AKR1C46.31
2Hyperaldosteronism, familial, type iEnrichmentCYP11B1, CYP11B24.83
3Lipoid congenital adrenal hyperplasiaEnrichmentCYP11B1, CYP21A24.05
446,xy disorder of sex development due to 5-alpha-reductase 2 deficiencyEnrichmentSRD5A23.35
5Xanthinuria, type iEnrichmentSRD5A23.05
6Cic-rearranged sarcomaEnrichmentAKR1C23.05
7Bile acid synthesis defect, congenital, 2EnrichmentAKR1D12.99
8Apparent mineralocorticoid excessEnrichmentHSD11B22.99
9Vitamin d-dependent rickets, type 3EnrichmentCYP3A42.99
10Corticosterone methyloxidase type i deficiencyEnrichmentCYP11B22.69
11Corticosterone methyloxidase type ii deficiencyEnrichmentCYP11B22.69
12Congenital bile acid synthesis defectEnrichmentAKR1D12.69
13Cortisone reductase deficiency 2EnrichmentHSD11B12.69
14Cortisone reductase deficiencyEnrichmentHSD11B12.69
15Familial hypoaldosteronismEnrichmentCYP11B22.69
16Early-onset familial hypoaldosteronismEnrichmentCYP11B22.69
17Pseudovaginal perineoscrotal hypospadiasEnrichmentSRD5A22.66
18Developmental dysplasia of the hip 1EnrichmentAKR1C12.58
19Adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiencyEnrichmentCYP11B12.51
20Deficiency of steroid 11-beta-monooxygenaseEnrichmentCYP11B12.51
21Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyEnrichmentCYP21A22.21
2221-hydroxylase-deficient congenital adrenal hyperplasiaEnrichmentCYP21A22.21
23Prostate cancerEnrichmentSRD5A21.89
24Autism spectrum disorderEnrichmentSRD5A21.33

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