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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

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

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Sub-types

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

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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