1.14.15.5: corticosterone 18-monooxygenase
This is an abbreviated version!
For detailed information about corticosterone 18-monooxygenase, go to the full flat file.
Word Map on EC 1.14.15.5
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1.14.15.5
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aldosterone
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18-hydroxycorticosterone
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steroid
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cyp11b2
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glomerulosa
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cortisol
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hypoaldosteronism
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zona
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thrive
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acth
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hyperkalemia
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renin
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18-hydroxylation
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salt-wasting
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mineralocorticoid
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fasciculata
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11-deoxycorticosterone
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18-hydroxycortisol
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18-oh-corticosterone
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fludrocortisone
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salt-losing
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18-oxocortisol
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furosemide
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p450aldo
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deoxycorticosterone
- 1.14.15.5
- aldosterone
- 18-hydroxycorticosterone
- steroid
- cyp11b2
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glomerulosa
- cortisol
- hypoaldosteronism
- zona
-
thrive
- acth
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hyperkalemia
- renin
-
18-hydroxylation
-
salt-wasting
-
mineralocorticoid
-
fasciculata
- 11-deoxycorticosterone
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18-hydroxycortisol
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18-oh-corticosterone
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fludrocortisone
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salt-losing
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18-oxocortisol
- furosemide
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p450aldo
- deoxycorticosterone
Reaction
+ 2 reduced adrenodoxin + + 2 H+ = + 2 oxidized adrenodoxin +
Synonyms
corticosterone 18-hydroxylase, corticosterone methyl oxidase, CYP11B2, cytochrome P450 11B2, oxygenase, corticosterone 18-mono-
ECTree
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Disease
Disease on EC 1.14.15.5 - corticosterone 18-monooxygenase
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Adrenogenital Syndrome
CYP17- and CYP11B-dependent steroid hydroxylases as drug development targets.
cholinesterase deficiency
Genetic screening in the Persian Jewish community: A pilot study.
corticosterone 18-monooxygenase deficiency
Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency.
corticosterone 18-monooxygenase deficiency
Computational analysis of functional single nucleotide polymorphisms associated with the CYP11B2 gene.
corticosterone 18-monooxygenase deficiency
Congenital hypoaldosteronism: the Visser-Cost syndrome revisited.
corticosterone 18-monooxygenase deficiency
Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant.
corticosterone 18-monooxygenase deficiency
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997.
corticosterone 18-monooxygenase deficiency
Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II.
corticosterone 18-monooxygenase deficiency
Multisteroid analysis in children with terminal aldosterone biosynthesis defects.
corticosterone 18-monooxygenase deficiency
Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II.
corticosterone 18-monooxygenase deficiency
The effect of ACTH stimulation on plasma steroids in two patients with congenital hypoaldosteronism and in their relatives.
Dehydration
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy.
Diabetes Mellitus
Acquired partial corticosterone methyl oxidase type II defect in diabetes mellitus. Case of hyperreninemic hypoaldosteronism.
Disorders of Sex Development
CYP17- and CYP11B-dependent steroid hydroxylases as drug development targets.
Herpes Zoster
18-Hydroxy-11-deoxycortisol: a new steroid isolated from incubations of the adrenal with 11-deoxycortisol.
Hyperaldosteronism
Computational analysis of functional single nucleotide polymorphisms associated with the CYP11B2 gene.
Hypoaldosteronism
Acquired partial corticosterone methyl oxidase type II defect in diabetes mellitus. Case of hyperreninemic hypoaldosteronism.
Hypoaldosteronism
Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies.
steroid 11beta-monooxygenase deficiency
Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant.
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