abnormality of the fetal cardiovascular system Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the fetal circulation system or fetal echocardiogram. (Human Phenotype Ontology, HP_0010948)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010948
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Genes

10 genes associated with the abnormality of the fetal cardiovascular system 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