HMGB1, high mobility group box 1, 3146

N. diseases: 724; N. variants: 10
Disease: Hereditary persistence of fetal hemoglobin thalassemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		0.010 Biomarker disease BEFREE These findings implicate HMG-I in the HPFH phenotype; we speculate that it may participate in the formation of multiprotein complexes that regulate globin gene expression. 7575565 1995