|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A progressive form of scoliosis with congenital onset. (Human Phenotype Ontology, HP_0008458)|
|Downloads & Tools|
1 genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PLOD1||procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1|