progressive congenital scoliosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A progressive form of scoliosis with congenital onset. (Human Phenotype Ontology, HP_0008458)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008458
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Genes

1 genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1