CD19, CD19 molecule, 930

N. diseases: 328; N. variants: 2
Disease: Congenital chromosomal disease ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 Biomarker group BEFREE This is the first reported case of CD19-positive AML with trisomy 21 as the sole cytogenetic abnormality. 19882758 2009
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 GeneticVariation 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 		0.030 GeneticVariation group BEFREE Phenotypical characteristics of acute myelocytic leukemia associated with the t(8;21)(q22;q22) chromosomal abnormality: frequent expression of immature B-cell antigen CD19 together with stem cell antigen CD34. 1378322 1992