| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A reduced ability to secrete prolactin, a protein hormone that is secreted by lactotrophs in the anterior pituitary and that stimulates mammary gland development and milk production. (Human Phenotype Ontology, HP_0008202) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008202 |
| Similar Terms | |
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1 genes associated with the prolactin deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PROP1 | PROP paired-like homeobox 1 |
