SRL, sarcalumenin, 6345

N. diseases: 77; N. variants: 3
Disease: Congenital chromosomal disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.010 Biomarker group BEFREE Construction and application of (Q)SAR models to predict chemical-induced in vitro chromosome aberrations. 30278198 2018