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ENCorticosterone Methyloxidase Type I Deficiency (CMO-1 DEFICIENCY)
Alias:
Hypoaldosteronism, Congenital, Due to Cmo I Deficiency
Corticosterone Methyloxidase Deficiency 1
18-Hydroxylase Deficiency
Aldosterone Deficiency I
Cmo I Deficiency
Aldosterone Deficiency Due to Defect in Steroid 18-Hydroxylase
Aldosterone Deficiency Due to Defect in 18-Hydroxylase
Corticosterone Methyl Oxidase Type Ii Deficiency
Corticosterone Methyl Oxidase Type I Deficiency
Corticosterone Methyloxidase Type 1 Deficiency
Hyperreninemic Hypoaldosteronism, Familial, 1
Corticosterone 18-Monooxygenase Deficiency
Corticosterone Methyloxidase 1 Deficiency
Steroid 18-Hydroxylase Deficiency
Aldosterone Synthase Deficiency
18 Hydroxylase Deficiency
Cmo-1 Deficiency
Fhha1a
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Corticosterone Methyloxidase Type I Deficiency, also known as hypoaldosteronism, congenital, due to cmo i deficiency, is related to corticosterone methyloxidase type ii deficiency and corticosterone methyloxidase deficiency, and has symptoms including vomiting An important gene associated with Corticosterone Methyloxidase Type I Deficiency is CYP11B2 (Cytochrome P450 Family 11 Subfamily B Member 2), and among its related pathways/superpathways are Metabolism and Metapathway biotransformation Phase I and II. Affiliated tissues include adrenal gland, and related phenotypes are failure to thrive and hypotension
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