| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An acquired metabolic disease that has_material_basis_in the presence of abnormally-high levels of prolactin in the blood. (Human Disease Ontology, DOID_12700) |
| External Link | http://www.omim.org/entry/615555 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the ?hyperprolactinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PRLR | prolactin receptor |
