Ovalocytosis, Hereditary Hemolytic MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Ovalocytosis, Hereditary Hemolytic
Unique ID: C563480
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563480
Registry Numbers: 0
Heading Mapped to: *Elliptocytosis, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Ovalocytosis, Hereditary Hemolytic Preferred

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