abnormal maternal serum screening Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally elevated or decreased level of a maternal serum marker analytes used in screening for aneuploidy. (Human Phenotype Ontology, HP_0011436)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011436
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Genes

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.

Symbol Name
AFP alpha-fetoprotein
POR P450 (cytochrome) oxidoreductase