Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.050 AlteredExpression group BEFREE We describe an AML patient showing the chromosomal abnormality t(8;21) and CD56 expression who experienced a unique EM relapse after allo-HSCT. 19629629 2009
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.050 Biomarker group BEFREE Patients with this cytogenetic abnormality showed higher frequency of CD34 (P = 0.003), HLA-DR (P = 0.03), Tdt (P = 0.02), CD19 (P < 0.0001), and CD56 (P < 0.0001) and lower CD33 (P = 0.0001). 14692523 2003
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.050 Biomarker group BEFREE Patients with t(8;21) had a significantly higher incidence (89%, 8/9) of CD56 positivity in leukemic cells than those with normal karyotype or other cytogenetic abnormalities (26%, 22/85, p < 0.001). 12189644 2002
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.050 AlteredExpression group BEFREE Moreover, CD56 expression was significantly associated with P-glycoprotein (PGP) hyperexpression (P = 0.007), unfavorable cytogenetic abnormalities (P = 0.008) and with a reduced probability of achieving complete remission (CR) (36% vs 68%) (P = 0.035) as well as with a shorter survival (6 vs 12 months) (P = 0.032). 11480556 2001
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.050 Biomarker group BEFREE This study indicates that chromosome aberrations in NK-cell lymphomas are restricted to the CD56+, CD3- and CD5- cell population and that NK-cell lymphomas are indeed derived from mature true NK cells and not from T lymphocytes. 10354139 1999