Neutropenia, Severe Congenital, Autosomal Dominant 2 MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Neutropenia, Severe Congenital, Autosomal Dominant 2
Unique ID: C567748
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567748
Entry Term(s): Severe Congenital Neutropenia-2
Registry Number: 0
Heading Mapped to: *Neutropenia
Frequency: 0
Note: GFI1 mutations
Date of Entry: 2012/11/05

Neutropenia, Severe Congenital, Autosomal Dominant 2 Preferred

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