SMS, spermine synthase, 6611

N. diseases: 263; N. variants: 9
Disease: Congenital scoliosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0559260
Disease: Congenital scoliosis
Congenital scoliosis 		0.010 Biomarker disease BEFREE A prospective institutional CS database was queried to identify patients who had the EOSQ-24 and SRS-22 completed at the same time point. 31157754 2020