CD38, CD38 molecule, 952

N. diseases: 473; N. variants: 7
Disease: Chromosome 12, 12p trisomy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0795845
Disease: Chromosome 12, 12p trisomy
Chromosome 12, 12p trisomy 		0.010 AlteredExpression disease BEFREE NOTCH1 mutations correlated with a shorter treatment-free interval (p = 0.058), an unmutated immunoglobulin heavy variable gene (IGHV) status (p < 0.0001), CD38 and ZAP-70 expression (p = 0.0025 and 0.026, respectively) and trisomy 12 (p = 0.0028), SF3B1 mutations with an unmutated IGHV status (p = 0.02), and BIRC3 disruptions with an unmutated IGHV configuration (p = 0.01) and 11q deletion (p < 0.0001). 24597984 2014