# glucocorticoid deficiency 2

> human disease

**Wikidata**: [Q55999739](https://www.wikidata.org/wiki/Q55999739)  
**Source**: https://4ort.xyz/entity/glucocorticoid-deficiency-2


## References

1. Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
2. Monarch Disease Ontology release 2018-06-29
3. Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2
4. Emerging roles of melanocortin receptor accessory proteins (MRAP and MRAP2) in physiology and pathophysiology