Structured Summary
Abstract
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
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Synonyms
1 entry terms
- Hemoglobinopathy
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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
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History Note
68
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NLM Classification
WH 190
AMA Style
References
- National Library of Medicine. Hemoglobinopathies. Medical Subject Headings (MeSH). 2026. Unique ID D006453. http://id.nlm.nih.gov/mesh/2026/D006453
- Hemoglobinopathies. In: Wikipedia. https://en.wikipedia.org/wiki/Hemoglobinopathy
- Hemoglobinopathies. In: Wikidata. https://www.wikidata.org/wiki/Q1642147