Familial glucocorticoid deficiency

MONDO:0008733

Familial glucocorticoid deficiency (FGD) is a group of primary adrenal insufficiencies characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections, and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency.

Also known as: glucocorticoid deficiency, GCCD

2 clinical trials for this condition and its sub-types, 0 tagged with Familial glucocorticoid deficiency itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18235) ↑ Chronic primary adrenal insufficiency (47)

Sub-types of Familial glucocorticoid deficiency

Adrenocortical unresponsiveness to ACTH with postreceptor defect 0 trials
Glucocorticoid deficiency 1 0 trials
Glucocorticoid deficiency 2 0 trials
Glucocorticoid deficiency 3 0 trials
Glucocorticoid deficiency 4 0 trials
Glucocorticoid deficiency 5 0 trials

Including sub-types (2) Tagged with Familial glucocorticoid deficiency (0)

Trials to join now! 1 Not yet recruiting 1

Tiny trial to see if a dye helps adrenal surgery

Knowledge-focused Not yet recruiting

This study will look at 12 people having surgery to remove an adrenal gland (adrenalectomy) using robotic or laparoscopic methods. Some surgeries will use a green dye called Indocyanine Green (ICG) to help the surgeon see better, while others will not. The main goal is to track c…

Sponsor: University of Roma La Sapienza • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:32 UTC

Familial glucocorticoid deficiency

Where it sits in the disease tree

Tiny trial to see if a dye helps adrenal surgery