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Hyper-IgM Immunodeficiency Syndrome, Type 1 MeSH Descriptor Data 2022


MeSH Heading
Hyper-IgM Immunodeficiency Syndrome, Type 1
Tree Number(s)
C15.378.147.333.249.500
C16.320.322.237
C16.320.798.625.500
C20.673.430.250.500
C20.673.795.625.500
Unique ID
D053307
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D053307
Scope Note
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
Entry Term(s)
HIGM1
HIGM1 Syndrome
Hyper-IgM Immunodeficiency, X-Linked
Hyper-IgM Syndrome 1
Immunodeficiency with Hyper-IgM, Type 1
X-Linked Hyper IgM Syndrome
Previous Indexing
CD40 Ligand (2000-2006)
Immunologic Deficiency Syndromes (1995-2006)
Public MeSH Note
2007
History Note
2007
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2019/06/17
Hyper-IgM Immunodeficiency Syndrome, Type 1 Preferred
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