delta beta-thalassemia

Summary
Definition
A beta thalassemia that is characterized by decreased or absent synthesis of both the delta- and beta-globin chains, which leads to a compensatory increase in fetal gamma-chain synthesis. This disorder results in a microcytic anemia that is clinically mild.
Super Class
autosomal dominant disease beta thalassemia
Disease Ontology
DOID:0080773
NCI Thesaurus
ORDO
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3043 HBB hemoglobin subunit beta

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024