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ENCorticosterone Methyloxidase Type Ii Deficiency (CMO-2 DEFICIENCY)
Alias:
Hypoaldosteronism, Congenital, Due to Cmo Ii Deficiency
Corticosterone Methyl Oxidase Type Ii Deficiency
Corticosterone Methyloxidase Type 2 Deficiency
Aldosterone Deficiency Due to Deficiency of Steroid 18-Oxidase
Corticosterone Methyl Oxidase Type I Deficiency
Hyperreninemic Hypoaldosteronism, Familial, 1
Corticosterone Methyloxidase 2 Deficiency
Steroid 18-Oxidase Deficiency
Aldosterone Deficiency Ii
18-Oxidase Deficiency
Cmo Ii Deficiency
Cmo-2 Deficiency
Fhha1b
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Corticosterone Methyloxidase Type Ii Deficiency, also known as hypoaldosteronism, congenital, due to cmo ii deficiency, is related to corticosterone methyloxidase type i deficiency and hypoaldosteronism, and has symptoms including vomiting An important gene associated with Corticosterone Methyloxidase Type Ii Deficiency is CYP11B2 (Cytochrome P450 Family 11 Subfamily B Member 2). Related phenotypes are hyponatremia and hyperkalemia
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