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Glucocorticoid deficiency 4

MONDO:0013874

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

Also known as: NNT familial glucocorticoid deficiency, familial glucocorticoid deficiency caused by mutation in NNT, glucocorticoid deficiency 4, glucocorticoid deficiency 4, with or without mineralocorticoid deficiency, glucocorticoid deficiency type 4, GCCD4, glucocorticoid deficiency 4 with or without mineralocorticoid deficiency

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

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Broader categories

Disease (680) Hereditary disease (176) Endocrine system disorder (72) Adrenocortical insufficiency (26) Human disease (14) Adrenal gland disorder (8) Chronic primary adrenal insufficiency (5) Primary adrenal insufficiency (4) Disease of genetic or genomic mechanism (2) Adrenal cortex disorder (0)
Trials to join now! 1 Not yet recruiting 1
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  • New imaging tracer could shed light on adrenal cholesterol

    Knowledge-focused Recruiting now

    This study tests a special radioactive tracer called [18F]FNP-59 to see if it can safely and clearly show cholesterol activity in the adrenal gland using PET scans. About 24 people will take part, including healthy volunteers and those with known adrenal problems. The goal is to …

    Phase: EARLY_PHASE1 • Sponsor: Benjamin Viglianti • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:02 UTC

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