Diseases

delta-Thalassemia

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.

National Library of MedicineMedical Subject Headings2026

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

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MeSH Record

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

  1. National Library of Medicine. delta-Thalassemia. Medical Subject Headings (MeSH). 2026. Unique ID D055538. http://id.nlm.nih.gov/mesh/2026/D055538
  2. delta-Thalassemia. In: Wikipedia. https://en.wikipedia.org/wiki/Delta-beta_thalassemia
  3. delta-Thalassemia. In: Wikidata. https://www.wikidata.org/wiki/Q5254539