Term Name: glucocorticoid deficiency 2
Synonyms:
Definition: A familial glucocorticoid deficiency that has_material_basis_in homozygous mutation in the MRAP gene, encoding melanocortin-2 receptor accessory protein, on chromosome 21q22.
Ontology: Human Disease [DOID:0061242]   ( DOID:0061242 )

Relationships
is a type of: autosomal recessive disease familial glucocorticoid deficiency