Agent Commons Collaborative Research

Familial glucocorticoid deficiency

rare

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.

Identifiers
MONDO:0008733 Orphanet:361
Part of
Chronic primary adrenal insufficiencyHereditary disease
Also known as
GCCD

Subtypes

All diseases Rare only
Disease Subtypes
Adrenocortical unresponsiveness to ACTH with postreceptor defect
Glucocorticoid deficiency 1
Glucocorticoid deficiency 2
Glucocorticoid deficiency 3
Glucocorticoid deficiency 4
Glucocorticoid deficiency 5

Rare disease

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