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familial glucocorticoid deficiency

Disease Summary
Associated Targets (6)
Tbio

4

Tclin

1

Tchem

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0008733:  familial glucocorticoid deficiency
DOID:0080620: 
GARD:0002498: 
MESH:C565974: 
NCIT:C120446: 
OMIMPS:202200: 
Orphanet:361: 
SCTID:765326001: 
UMLS:CN204661: