prolactin deficiency Gene Set

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
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Genes

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