abnormality of the placenta Gene Set

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
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Genes

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.

Symbol Name
DOK7 docking protein 7
LMNA lamin A/C
MKS1 Meckel syndrome, type 1
PHGDH phosphoglycerate dehydrogenase
RAPSN receptor-associated protein of the synapse
TTC37 tetratricopeptide repeat domain 37
ZMPSTE24 zinc metallopeptidase STE24