|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormal development of the neurohypophysis during embryonic growth and development. (Human Phenotype Ontology, HP_0011753)|
|Downloads & Tools|
3 genes associated with the posterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.