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Corticosterone methyloxidase type 1 deficiency

MONDO:0008751

Also known as: corticosterone 18-monooxygenase deficiency, corticosterone methyloxidase type 1 deficiency, hypoaldosteronism, congenital, due to cmo i deficiency, 18 Hydroxylase deficiency, 18 alpha hydroxylase deficiency, 18-Hydroxylase deficiency, 18-hydroxycorticosterone dehydrogenase deficiency, 18-hydroxylase deficiency

3 clinical trials for this condition and its sub-types, 0 tagged with Corticosterone methyloxidase type 1 deficiency itself.

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Part of

↑ Inherited lipid metabolism disorder (644) ↑ Steroid metabolism disease (104) ↑ Familial hypoaldosteronism (0)

Including sub-types (3) Tagged with Corticosterone methyloxidase type 1 deficiency (0)

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