abnormalities of placenta or umbilical cord 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) or of the umbilical cord (the cord that connects the fetus to the placenta). (Human Phenotype Ontology, HP_0001194)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001194
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25 genes associated with the abnormalities of placenta or 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
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
DOK7 docking protein 7
FANCB Fanconi anemia, complementation group B
FERMT1 fermitin family member 1
FOXF1 forkhead box F1
GATA6 GATA binding protein 6
GJB2 gap junction protein, beta 2, 26kDa
GLE1 GLE1 RNA export mediator
HOXD13 homeobox D13
KIAA0196 KIAA0196
LMNA lamin A/C
MKS1 Meckel syndrome, type 1
NSDHL NAD(P) dependent steroid dehydrogenase-like
PHGDH phosphoglycerate dehydrogenase
POMP proteasome maturation protein
POR P450 (cytochrome) oxidoreductase
RAPSN receptor-associated protein of the synapse
SCARF2 scavenger receptor class F, member 2
TTC37 tetratricopeptide repeat domain 37
VANGL1 VANGL planar cell polarity protein 1
WNT3 wingless-type MMTV integration site family, member 3
ZMPSTE24 zinc metallopeptidase STE24