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Glucocorticoid deficiency 1

MONDO:0024536

Any familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MC2R gene.

Also known as: MC2R familial glucocorticoid deficiency, familial glucocorticoid deficiency caused by mutation in MC2R, glucocorticoid deficiency 1, glucocorticoid deficiency, due to ACTH unresponsiveness, ACTH resistance, GCCD1, adrenal unresponsiveness to ACTH, familial glucocorticoid deficiency 1

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

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Broader categories

Disease (618) Hereditary disease (172) Endocrine system disorder (61) Adrenocortical insufficiency (23) Human disease (14) Adrenal gland disorder (8) Chronic primary adrenal insufficiency (4) Primary adrenal insufficiency (3) Disease of genetic or genomic mechanism (2) Adrenal cortex disorder (0)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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  • Researchers measure breathing, strength, and quality of life in hospitalized endocrine patients

    Knowledge-focused Completed

    This completed observational study at Uşak University examined 150 adults hospitalized in the endocrinology department. Researchers measured breathing, muscle strength, pain, fatigue, sleep quality, physical activity, balance, and nerve function. The goal was to better understand…

    Sponsor: Uşak University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:30 UTC

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