Neutropenia, Severe Congenital, X-Linked MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Neutropenia, Severe Congenital, X-Linked
Unique ID: C564539
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564539
Heading Mapped to: Neutropenia / congenital; *Genetic Diseases, X-Linked
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Neutropenia, Severe Congenital, X-Linked Preferred

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