GLUCOCORTICOID DEFICIENCY 3 (GCCD3)

Question 1

What is  GLUCOCORTICOID DEFICIENCY 3 (GCCD3)?

Accepted Answer

very rare

autosomal recessive

Question 2

What is the link to OMIM ?

Accepted Answer

OMIN 609197

Disease	GLUCOCORTICOID DEFICIENCY 3 (GCCD3)
Synonym	FAMILIAL GLUCOCORTICOID DEFICIENCY 3; FGD3
OMIM	609197 OMIM = Online Mendelian Inheritance of Men
Orphanet	361
Gene locus	8q11.2-q13.2
ICD	E27.1
Summary	very rare autosomal recessive
Laboratory findings	Adrenocorticotropic hormone (ACTH) inc (plasma) Cortisol dec (plasma) D-Glucose dec (serum)
Symptoms	hyperpigmentation hypoglycemia onset, adolescent onset, childhood onset, infancy