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Hemoglobin C Disease MeSH Descriptor Data 2023


MeSH Heading
Hemoglobin C Disease
Tree Number(s)
C15.378.071.141.150.490
C15.378.420.463
C16.320.070.490
C16.320.365.463
Unique ID
D006445
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006445
Annotation
a congen hemolytic anemia; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES; do not confuse with HEMOGLOBIN SC DISEASE
Scope Note
A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
Entry Version
HEMOGLOBIN C DIS
Entry Term(s)
Hemoglobin-C Disease
Public MeSH Note
1972
History Note
1972(1966)
Date Established
1972/01/01
Date of Entry
1999/01/01
Revision Date
2009/07/06
Hemoglobin C Disease Preferred
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