This is just here as a test because I lose it

Term information

importedFrom

http://purl.obolibrary.org/obo/MONDO_0014421

oboInOwl:hasDbXRef

https://www.ncbi.nlm.nih.gov/pubmed/19906237

oboInOwl:hasDefinition

An autosomal dominant condition due to mutation(s) in the NR3C1 gene, encoding the glucocorticoid receptor, resulting in decreased receptor affinity to glucocorticoids. Compensatory activation of the hypothalamic- pituitary-adrenal (HPA) axis results in increased mineralocorticoid and androgen production; clinical manifestations of glucocorticoid deficiency are rare.

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