abnormality of the umbilical cord Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the umbilical cord, which is the cord connecting the developing embryo or fetus to the placenta. (Human Phenotype Ontology, HP_0010881)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010881
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Genes

15 genes associated with the abnormality of the umbilical cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC22 coiled-coil domain containing 22
DOK7 docking protein 7
FANCB Fanconi anemia, complementation group B
FOXF1 forkhead box F1
GATA6 GATA binding protein 6
HOXD13 homeobox D13
KIAA0196 KIAA0196
LMNA lamin A/C
MKS1 Meckel syndrome, type 1
PHGDH phosphoglycerate dehydrogenase
RAPSN receptor-associated protein of the synapse
SCARF2 scavenger receptor class F, member 2
VANGL1 VANGL planar cell polarity protein 1
WNT3 wingless-type MMTV integration site family, member 3
ZMPSTE24 zinc metallopeptidase STE24