Metabolism of steroid hormones

Pathway network for the Metabolism of steroid hormones SuperPath

Sources:
  • Reactome
  • WikiPathways

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

Disorders associated with Metabolism of steroid hormones SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Adrenal insufficiency, congenital, with 46,xy sex reversal, partial or completeDirect
2Adrenal gland diseaseDirect
3Lipoid congenital adrenal hyperplasiaEnrichmentCYP11A1, CYP11B1, CYP17A1, CYP21A2, HSD3B2, STAR16.00
4Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyEnrichmentCYP11A1, CYP17A1, CYP21A28.56
521-hydroxylase-deficient congenital adrenal hyperplasiaEnrichmentCYP11A1, CYP17A1, CYP21A28.56
6Hyperaldosteronism, familial, type iEnrichmentCYP11B1, CYP11B25.14
7Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndromeEnrichmentFDXR3.66
8Hypogonadotropic hypogonadism 23 with or without anosmiaEnrichmentLHB3.35
9Apparent mineralocorticoid excessEnrichmentHSD11B23.23
10Inherited isolated adrenal insufficiency due to partial cyp11a1 deficiencyEnrichmentCYP11A13.23
11Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathyEnrichmentFDX23.18
12Auditory neuropathy and optic atrophyEnrichmentFDXR3.18
13Multiple mitochondrial dysfunctions syndrome 9bEnrichmentFDXR3.18
14Corticosteroid-binding globulin deficiencyEnrichmentSERPINA63.13
15Kahrizi syndromeEnrichmentSRD5A33.09
1646,xy disorder of sex development due to 5-alpha-reductase 2 deficiencyEnrichmentSRD5A23.09
17Corticosterone methyloxidase type i deficiencyEnrichmentCYP11B23.05
18Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiencyEnrichmentHSD3B23.05
19Corticosterone methyloxidase type ii deficiencyEnrichmentCYP11B23.05
20Hypospadias 1, x-linkedEnrichmentHSD3B23.05
213 beta-hydroxysteroid dehydrogenase deficiencyEnrichmentHSD3B23.05
22Familial hypoaldosteronismEnrichmentCYP11B23.05
23Early-onset familial hypoaldosteronismEnrichmentCYP11B23.05
24Dystonia 22, adult-onsetEnrichmentTSPOAP13.05
25Non-classic congenital lipoid adrenal hyperplasia due to star deficencyEnrichmentSTAR3.05
26Classic congenital lipoid adrenal hyperplasia due to star deficencyEnrichmentSTAR3.05
27Cortisone reductase deficiency 2EnrichmentHSD11B12.93
28Cortisone reductase deficiencyEnrichmentHSD11B12.93
29Aromatase excess syndromeEnrichmentCYP19A12.88
30Aromatase deficiencyEnrichmentCYP19A12.88
31Xanthinuria, type iEnrichmentSRD5A22.79
3217-beta hydroxysteroid dehydrogenase iii deficiencyEnrichmentHSD17B32.79
33Congenital disorder of glycosylation, type iqEnrichmentSRD5A32.79
34Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiencyEnrichmentCYP17A12.75
35Toe syndactyly, telecanthus, and anogenital and renal malformationsEnrichmentSTAR2.75
36Segawa syndrome, autosomal recessiveEnrichmentTSPOAP12.75
37Dystonia 22, juvenile-onsetEnrichmentTSPOAP12.75
38Adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiencyEnrichmentCYP11B12.66
39Obesity, early-onset, with adrenal insufficiency and red hairEnrichmentPOMC2.66
40Deficiency of steroid 11-beta-monooxygenaseEnrichmentCYP11B12.66
41Obesity due to pro-opiomelanocortin deficiencyEnrichmentPOMC2.66
42Mitochondrial myopathyEnrichmentFDX22.61
43Syndromic recessive x-linked ichthyosisEnrichmentSTS2.58
44Pseudovaginal perineoscrotal hypospadiasEnrichmentSRD5A22.39
45PseudohermaphroditismEnrichmentHSD17B32.39
46Familial glucocorticoid deficiencyEnrichmentSTAR2.35
47Ichthyosis, x-linkedEnrichmentSTS2.28
48Auditory neuropathyEnrichmentFDXR2.24
49Difference of sex developmentEnrichmentHSD17B32.19
50Optic nerve diseaseEnrichmentSRD5A32.09
51Epilepsy, myoclonic juvenileEnrichmentHSD17B32.05
52Primary ovarian insufficiencyEnrichmentCYP17A1, CYP19A11.97
53Congenital disorder of glycosylation, type inEnrichmentSRD5A31.86
54Cone dystrophyEnrichmentSRD5A31.71
55Prostate cancerEnrichmentSRD5A21.63
56Body mass index quantitative trait locus 11EnrichmentPOMC1.44
57Bardet-biedl syndromeEnrichmentTSPOAP11.44
58Breast cancerEnrichmentCYP17A11.36
59AutismEnrichmentSRD5A31.25
60Congenital nervous system abnormalityEnrichmentSRD5A31.08
61Nervous system diseaseEnrichmentSRD5A31.08
62Autism spectrum disorderEnrichmentSRD5A21.07

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