delta-beta thalassemia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Delta-beta-thalassemia is a form of beta-thalassemia (see this term) characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis. (Orphanet Rare Disease Ontology, Orphanet_231237)
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1 genes associated with the delta-beta thalassemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HBB hemoglobin, beta