NLM Logo

Neutropenia, Severe Congenital, Autosomal Dominant 2 MeSH Supplementary Concept Data 2025


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 Numbers
0
Heading Mapped to
*Neutropenia
Frequency
0
Note
GFI1 mutations
Date of Entry
2012/11/05
Revision Date
1955/01/01
Neutropenia, Severe Congenital, Autosomal Dominant 2 Preferred
page delivered in 0.002s