|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the placenta, the organ that connects the developing fetus to the uterine wall to enable nutrient uptake, waste elimination, and gas exchange. (Human Phenotype Ontology, HP_0100767)|
|Downloads & Tools|
7 genes associated with the abnormality of the placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.