Human genes for glucocorticoid deficiency 1
Glucocorticoid deficiency 1 [DOID:0080621]
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.
Synonyms: glucocorticoid deficiency 1, DOID:0080621