Familial glucocorticoid deficiency

Orpha code: 361OMIM code: 617825

Definition

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.

Disease data
Classification

Disease

ORPHA code
361
OMIM code
617825
ICD10 code
E27.1
ICD11 code
5A74.Y

No additional description.

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