ALB, albumin, 213

N. diseases: 1198; N. variants: 21
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
0.070 Biomarker group BEFREE The recently introduced Revised International Staging System (R-ISS) for multiple myeloma (MM) integrates albumin, β2 microglobulin, lactate dehydrogenase (LDH) with high-risk cytogenetic aberrations (CA), i.e., t(4;14) and t(14;16) and del17p using fluorescent in situ hybridization (FISH). 30056581 2018
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 AlteredExpression group BEFREE Our study demonstrated that BD regimen was effective and well tolerated in newly diagnosed MM patients, and prognostic factors for patients' survival include level of albumin, plasma cell percentage in bone marrow, β<sub>2</sub>-microglobulin and cytogenetic abnormalities. 28883741 2017
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 Biomarker group BEFREE Both cell lines showed typical hepatocyte-like morphology under phase-contrast and electron microscopy and expressed alpha-fetoprotein, albumin, transferrin, and aldolase B. Cytogenetic analysis revealed extensive chromosomal anomalies. 23734258 2013
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 AlteredExpression group BEFREE On the other hand, CDDP significantly increased the levels of urea and creatinine and decreased the levels of albumin and total protein.The treatment of CCE before or after treatment with CDDP showed, (i) a total reduction of CDDP induced oxidative damage for all tested markers, (ii) an anti-genotoxic effect resulting in an efficient prevention of chromosomal aberrations compared to the group treated with CDDP alone (iii) restriction of the effect of CDDP by differential modulation of the expression of p53 which is decreased as well as its associated genes such as bax and bcl2, (iiii) restriction of serums levels of creatinine, urea, albumin and total protein resuming its values towards near normal levels of control. 22849573 2012
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 Biomarker group BEFREE As a group, these patients more often had low hemoglobin, high beta-2-microglobulin, high lactate dehydrogenase, low albumin and cytogenetic abnormalities. 22508408 2012
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 AlteredExpression group BEFREE MRI-FL correlated with low albumin and elevated levels of C-reactive protein, lactate dehydrogenase, and creatinine, but did not correlate with age, beta-2-microglobulin, and CA. 17296972 2007
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
0.070 Biomarker group BEFREE Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitation. 1955544 1991