humeroradial synostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal osseous union (fusion) between the radius and the humerus. (Human Phenotype Ontology, HP_0003041)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003041
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Genes

9 genes associated with the humeroradial synostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
FGF9 fibroblast growth factor 9
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
GDF5 growth differentiation factor 5
NOG noggin
POR P450 (cytochrome) oxidoreductase
PTDSS1 phosphatidylserine synthase 1
WNT7A wingless-type MMTV integration site family, member 7A