single umbilical artery Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Single umbilical artery (SUA) is the absence of one of the two umbilical arteries surrounding the fetal bladder and in the fetal umbilical cord. (Human Phenotype Ontology, HP_0001195)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001195
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Genes

10 genes associated with the single umbilical artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC22 coiled-coil domain containing 22
FANCB Fanconi anemia, complementation group B
FOXF1 forkhead box F1
GATA6 GATA binding protein 6
HOXD13 homeobox D13
KIAA0196 KIAA0196
MKS1 Meckel syndrome, type 1
SCARF2 scavenger receptor class F, member 2
VANGL1 VANGL planar cell polarity protein 1
WNT3 wingless-type MMTV integration site family, member 3