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Anemia, Hemolytic, Congenital Nonspherocytic MeSH Descriptor Data 2025


MeSH Heading
Anemia, Hemolytic, Congenital Nonspherocytic
Tree Number(s)
C15.378.050.141.150.100
C16.320.070.100
Unique ID
D000746
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000746
Scope Note
Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
Entry Version
ANEMIA HEMOL CONGEN NONSPHER
Entry Term(s)
Anemia, Congenital Nonspherocytic Hemolytic
Anemia, Hemolytic Congenital, Nonspherocytic
Congenital Nonspherocytic Hemolytic Anemia
Hemolytic Anemia, Congenital Nonspherocytic
Public MeSH Note
91,68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67
Online Note
use ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC to search ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1966-67
History Note
91(82)68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67
Date Established
1968/01/01
Date of Entry
1999/01/01
Revision Date
2023/02/26
Anemia, Hemolytic, Congenital Nonspherocytic Preferred
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