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Hemoglobin, Sickle MeSH Descriptor Data 2024


MeSH Heading
Hemoglobin, Sickle
Tree Number(s)
D12.776.124.400.463.588
D12.776.422.316.762.426.588
Unique ID
D006451
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006451
Annotation
/urine: coord IM with HEMOGLOBINURIA (IM); hemoglobin S disease = ANEMIA, SICKLE CELL
Scope Note
An abnormal hemoglobin resulting from the substitution of valine for glutamic acid at position 6 of the beta chain of the globin moiety. The heterozygous state results in sickle cell trait, the homozygous in sickle cell anemia.
Entry Version
HBS
Entry Term(s)
Deoxygenated Sickle Hemoglobin
Deoxyhemoglobin S
Hemoglobin S
Hemoglobin SS
Previous Indexing
Hemoglobins, Abnormal (1966-1972)
Public MeSH Note
77
Online Note
use HEMOGLOBIN, SICKLE to search HEMOGLOBIN S 1973-74 (as Prov)
History Note
77(75); was HEMOGLOBIN S 1973-74 (Prov)
Date Established
1977/01/01
Date of Entry
1999/01/01
Revision Date
2019/05/24
Hemoglobin, Sickle Preferred
Deoxyhemoglobin S Narrower
Hemoglobin SS Narrower
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