Glucocorticoid deficiency 1 is an adrenocortical failure characterized by low levels of plasma cortisol produced by the adrenal gland despite high levels of plasma ACTH . This is an inherited disorder with several different causes which define the type.
3-477: FGD may refer to: Familial glucocorticoid deficiency Fderik Airport , in Mauritania Flue-gas desulfurization Focus group discussion Functional generative description , a linguistic framework FYVE, RhoGEF and PH domain containing Topics referred to by the same term [REDACTED] This disambiguation page lists articles associated with
6-509: Is caused by mutations in the ACTH receptor (melanocortin 2 receptor; MC2R). FGD type 2 is caused by mutations in the MC2R accessory protein (MRAP). These two types account for 45% of all cases of FGD. Some cases of FGD type 3 are caused by mutations in the steroidogenic acute regulatory protein (StAR), with similarity to the nonclassic form of lipoid congenital adrenal hyperplasia . In this case,
9-486: The title FGD . If an internal link led you here, you may wish to change the link to point directly to the intended article. Retrieved from " https://en.wikipedia.org/w/index.php?title=FGD&oldid=1029123039 " Category : Disambiguation pages Hidden categories: Short description is different from Wikidata All article disambiguation pages All disambiguation pages Familial glucocorticoid deficiency FGD type 1 (FGD1 or GCCD1)
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