Corticosterone methyloxidase type 2 deficiency

MONDO:0012524

Also known as: hypoaldosteronism, congenital, due to CMO II deficiency, 18-oxidase deficiency, Cmo 2 deficiency, aldosterone deficiency 2, aldosterone deficiency due to deficiency of steroid 18-oxidase, corticosterone methyloxidase type II deficiency, hyperreninemic hypoaldosteronism, familial, 1, steroid 18-oxidase deficiency

3 clinical trials for this condition and its sub-types, 0 tagged with Corticosterone methyloxidase type 2 deficiency itself.

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↑ Hereditary disease (18235) ↑ Familial hypoaldosteronism (0)

Including sub-types (3) Tagged with Corticosterone methyloxidase type 2 deficiency (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.