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Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis MeSH Supplementary Concept Data 2023


MeSH Supplementary
Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
Unique ID
C563479
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563479
Registry Number
0
Heading Mapped to
*Elliptocytosis, Hereditary
Frequency
0
Date of Entry
2012/11/05
Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis Preferred
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