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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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)

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