| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Abnormally reduced levels of aldosterone. (Human Phenotype Ontology, HP_0004319) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D006994 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Hypoaldosteronism from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| CYP11B2 | cytochrome P450, family 11, subfamily B, polypeptide 2 | 2.88009 |
