Structured Summary
Abstract
A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of HEMOGLOBIN A2, a minor component of adult hemoglobin monitored in the diagnosis of BETA-THALASSEMIA.
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Classification
Broader headings
Related Concepts
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Synonyms
2 entry terms
- delta Thalassemia
- delta-Thalassemias
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
delta-beta thalassemia = DELTA-THALASSEMIA + BETA-THALASSEMIA
MeSH Record
History Note
2009
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. delta-Thalassemia. Medical Subject Headings (MeSH). 2026. Unique ID D055538. http://id.nlm.nih.gov/mesh/2026/D055538
- delta-Thalassemia. In: Wikipedia. https://en.wikipedia.org/wiki/Delta-beta_thalassemia
- delta-Thalassemia. In: Wikidata. https://www.wikidata.org/wiki/Q5254539