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Neutropenia, Severe Congenital, X-Linked MeSH Supplementary Concept Data 2022


MeSH Supplementary
Neutropenia, Severe Congenital, X-Linked
Unique ID
C564539
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564539
Registry Number
0
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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