| 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 ) |