Diseases

Hemoglobinopathies

A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

MeSH Record

Classification

Related Concepts

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See Also

MeSH Record

Synonyms

1 entry terms
  • Hemoglobinopathy

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

do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available

MeSH Record

History Note

68

MeSH Hierarchy

Tree Numbers

MeSH Record

NLM Classification

WH 190

AMA Style

References

  1. National Library of Medicine. Hemoglobinopathies. Medical Subject Headings (MeSH). 2026. Unique ID D006453. http://id.nlm.nih.gov/mesh/2026/D006453
  2. Hemoglobinopathies. In: Wikipedia. https://en.wikipedia.org/wiki/Hemoglobinopathy
  3. Hemoglobinopathies. In: Wikidata. https://www.wikidata.org/wiki/Q1642147