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ENCorticosterone Methyloxidase Deficiency
Alias:
Corticosterone 18-Monooxygenase Deficiency
Aldosterone Deficiency Due to Deficiency of Steroid 18-Hydroxylase
Aldosterone Deficiency Due to Deficiency of Steroid 18-Oxidase
Corticosterone Methyl Oxidase Type Ii Deficiency
Corticosterone Methyl Oxidase Type I Deficiency
Familial Hyperreninemic Hypoaldosteronism
Corticosterone Methyl Oxidase Deficiency
Steroid 18-Hydroxylase Deficiency
Aldosterone Synthase Deficiency
Steroid 18-Oxidase Deficiency
Congenital Hypoaldosteronism
18-Hydroxylase Deficiency
Aldosterone Deficiency
18-Oxidase Deficiency
Visser-Cost Syndrome
Hypoaldosteronism
Cmo Deficiency
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Corticosterone Methyloxidase Deficiency, also known as corticosterone 18-monooxygenase deficiency, is related to corticosterone methyloxidase type i deficiency and hypoaldosteronism, and has symptoms including vomiting An important gene associated with Corticosterone Methyloxidase Deficiency is CYP11B2 (Cytochrome P450 Family 11 Subfamily B Member 2). The drugs Fludrocortisone and Anti-Inflammatory Agents have been mentioned in the context of this disorder. Affiliated tissues include adrenal gland and adipocyte.
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