| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Apparent mineralocorticoid excess (AME) is a rare form of pseudohyperaldosteronism characterized by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism. (Orphanet Rare Disease Ontology, Orphanet_320) |
| External Link | http://www.omim.org/entry/218030 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the apparent mineralocorticoid excess phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HSD11B2 | hydroxysteroid (11-beta) dehydrogenase 2 |
