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Metadata
ID	DOID:0080621
Name	glucocorticoid deficiency 1
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. https://www.ncbi.nlm.nih.gov/pubmed/19500760
Xrefs	MIM:202200
Parent Relationships	is_a autosomal recessive disease is_a familial glucocorticoid deficiency
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance