Term Name:	glucocorticoid deficiency 1
Synonyms:
Definition:	A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding melanocortin-2 receptor, which is also referred to as adrenocorticotropin receptor, on chromosome 18p11.
Ontology:	Human Disease [DOID:0080621]   ( DOID:0080621 )