Neutropenia, Severe Congenital, Autosomal Dominant 1 MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Neutropenia, Severe Congenital, Autosomal Dominant 1
Unique ID: C565969
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565969
Registry Number: 0
Heading Mapped to: Neutropenia / *congenital
Frequency: 0
Note: PROM mutation in the neutrophil elastase gene ELANE
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Neutropenia, Severe Congenital, Autosomal Dominant 1 Preferred

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