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| Term | delta beta-thalassemia | ID (Ontology) | DOID:0080773 (Human Disease) |
| 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. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ thalassemia | |__beta thalassemia____________| delta beta-thalassemia |
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| Parents/Children View Depth |
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Relationships
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| Is a |
autosomal dominant disease beta thalassemia |
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External Crossreferences & Linkouts
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NCI:C172823 ORDO:231237 |
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