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Hemoglobinopathies MeSH Descriptor Data 2023


MeSH Heading
Hemoglobinopathies
Tree Number(s)
C15.378.420
C16.320.365
Unique ID
D006453
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006453
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
Scope Note
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
NLM Classification #
WH 190
See Also
Hemoglobins, Abnormal
Public MeSH Note
68
History Note
68
Date Established
1968/01/01
Date of Entry
1999/01/01
Revision Date
2001/07/25
Hemoglobinopathies Preferred
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