Progressive Congenital Scoliosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A progressive form of scoliosis with congenital onset. (Human Phenotype Ontology, HP_0008458)
External Link https://www.disgenet.org/browser/0/1/0/C1857025
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Genes

4 genes associated with the disease Progressive Congenital Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PTCH1 patched 1
SEMA6A sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
STAC3 SH3 and cysteine rich domain 3