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Anemia, Hemolytic, Congenital MeSH Descriptor Data 2024


MeSH Heading
Anemia, Hemolytic, Congenital
Tree Number(s)
C15.378.050.141.150
C16.320.070
Unique ID
D000745
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000745
Scope Note
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
Entry Version
ANEMIA HEMOLYTIC CONGEN
Entry Term(s)
Anemia, Hemolytic, Hereditary
Congenital Hemolytic Anemia
Hemolytic Anemia, Congenital
Hemolytic Anemia, Hereditary
Hereditary Hemolytic Anemia
NLM Classification #
WH 170
Public MeSH Note
68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC was heading 1968-81, was ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1965-67
Online Note
use ANEMIA, HEMOLYTIC, CONGENITAL to search ANEMIA, CONGENITAL HEMOLYTIC 1966-67
History Note
68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64
Date Established
1968/01/01
Date of Entry
1999/01/01
Revision Date
2023/02/26
Anemia, Hemolytic, Congenital Preferred
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