Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3043
Gene Symbol: HBB
HBB
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia 		0.400 GermlineCausalMutation ORPHANET Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population. 18932066

2008
Entrez Id: 3047
Gene Symbol: HBG1
HBG1
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia 		0.350 GermlineCausalMutation ORPHANET Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population. 18932066

2008
Entrez Id: 3045
Gene Symbol: HBD
HBD
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia 		0.350 GermlineCausalMutation ORPHANET A novel delta-thalassemia mutation A G-->C substitution at codon 30 of the delta-globin gene in a person of southern Italian origin. 1301204

1992