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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

9 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Endocrine system disorder (61) Human disease (14) Adrenal gland disorder (8) Disease of genetic or genomic mechanism (2) Hypoaldosteronism disease (1) Disease by body system or component (0) Disease by etiologic mechanism (0) Familial hypoaldosteronism (0)
Trials to join now! 6 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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  • Brain scans reveal hidden links between body diseases and metabolism

    Knowledge-focused Ongoing

    This study watches 200 people with lung, gut, or hormone diseases over time using special brain scans (PET). It aims to see how these diseases change brain activity and whether those changes can predict tumor return, spread, or survival. No new treatment is tested—just observatio…

    Sponsor: The First Affiliated Hospital of Zhengzhou University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:52 UTC

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