Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
0.050 Biomarker BEFREE Methemoglobinemia is a blood disorder in which an abnormal amount of methemoglobin (MetHb), a form of hemoglobin (Hb), is produced from either inadequate MetHb reductase activity or too much MetHb production or by exposure to oxidizing agents. 29245041

2018

Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
0.050 Biomarker BEFREE Thalassemia is a genetic blood disorder that causes abnormal hemoglobin. 28135306

2017

Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
0.050 Biomarker BEFREE Sickle cell anemia (SCA) is a common hematological disorder among individuals of African descent in the United States; the disorder results in the production of abnormal hemoglobin. 28115816

2017

Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
0.050 AlteredExpression BEFREE These data could have practical relevance, because pharmacologically mediated regulation of human gamma-globin gene expression, with the consequent induction of fetal hemoglobin, is considered a potential therapeutic approach in hematological disorders including beta-thalassemia and sickle cell anemia. 19777196

2009

Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
0.050 AlteredExpression BEFREE These results could have practical relevance, because pharmacologically mediated regulation of the expression of human gamma-globin genes, leading to increased HbF, is considered a potential therapeutic approach in haematological disorders, including beta-thalassaemia and sickle cell anaemia. 15287957

2004