HBZ, hemoglobin subunit zeta, 3050

N. diseases: 40; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 Biomarker disease BEFREE In this work, a fluorescence immunochromatographic assay (FL-ICA) was established to detect the zeta globin chain in the hemolysates of carriers of the (--(SEA)) α-thalassemia deletion. 22677106 2013
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 Biomarker disease BEFREE Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain. 22438184 2012
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 Biomarker disease BEFREE The aim of this study was to develop an appropriate low-cost ELISA for zeta-globin chain detection as a routine screening test for (--(SEA)) alpha thalassaemia deletion. 19181632 2009
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 Biomarker disease BEFREE We evaluated an enzyme-linked immunosorbent assay (ELISA) for embryonic zeta-globin chains as a routine screening test for (--(SEA)) alpha-thalassemia deletion (SEA deletion). 12145460 2002
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 Biomarker disease BEFREE Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia. 7490322 1995
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 GeneticVariation disease BEFREE The test appears to identify patients, such as those with the Thai and Filipino deletion variants, whose alpha-thalassemia cannot be definitively characterized by DNA testing when only alpha- and zeta-globin probes are used in the analysis. 1329692 1992
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 GeneticVariation disease BEFREE A dual restriction enzyme digestion protocol was development using a 3' zeta-globin probe to clearly distinguish the most common alpha-thalassemia deletions that represent nearly all the alpha-thalassemia haplotypes in Southeast Asia. 1975558 1990
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
0.080 GeneticVariation disease BEFREE In a gene mapping study on 217 newborn babies in Taiwan with alpha- and zeta-globin probes, we have observed 4 cases (1.84%) of alpha-thalassemia-2 heterozygotes (zeta zeta-alpha/zeta zeta alpha alpha) without increased levels of hemoglobin (Hb) Bart's in the cord blood. 2508397 1989