| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0100767 |
| Similar Terms | |
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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.
