MeSH Browser

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

Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis MeSH Supplementary Concept Data 2025