Erythroreticulosis, Hereditary Benign MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Erythroreticulosis, Hereditary Benign
Unique ID: C566285
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566285
Registry Numbers: 0
Heading Mapped to: *Anemia, Dyserythropoietic, Congenital
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Erythroreticulosis, Hereditary Benign Preferred

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