|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the prolactin deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PROP1||PROP paired-like homeobox 1|