|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormally elevated or decreased level of a maternal serum marker analytes used in screening for aneuploidy. (Human Phenotype Ontology, HP_0011436)|
|Downloads & Tools|
2 genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.