|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the delta-beta thalassemia phenotype from the curated OMIM Gene-Disease Associations dataset.