| Term Name: | apparent mineralocorticoid excess syndrome |
|---|---|
| Synonyms: | 11-beta-hydroxysteroid dehydrogenase deficiency type 2, cortisol 11-beta-ketoreductase deficiency, syndrome of apparent mineralocorticoid excess, Ulick syndrome |
| Definition: | A steroid inherited metabolic disorder characterized by decreased conversion of biologically active cortisol to inactive cortisone resulting in low aldosterone levels, metabolic alkalosis, hypernatremia, hypokalemia and early-onset severe hypertension that has_material_basis_in homozygous or compound heterozygous mutation in the HSD11B2 gene on chromosome 16. |
| Ontology: | Human Disease [DOID:4367] ( DOID:4367 ) |