glucocorticoid deficiency 1 (DOID:0080621)
Alliance: disease page
Alt IDs: OMIM:202200
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.