Disease: Trisomy 12 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0432408
Disease: Trisomy 12
Trisomy 12 		0.010 GeneticVariation phenotype BEFREE Although most genetic alterations are not associated with consistent epigenetic profiles, CLLs with MYD88 mutations and trisomy 12 show distinct chromatin configurations. 29785028 2018