short umbilical cord Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased length of the umbilical cord. (Human Phenotype Ontology, HP_0001196)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001196
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Genes

5 genes associated with the short umbilical cord 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
PHGDH phosphoglycerate dehydrogenase
RAPSN receptor-associated protein of the synapse
ZMPSTE24 zinc metallopeptidase STE24