Mesh term Hyper-IgM Immunodeficiency Syndrome, Type 1
Browse to parent terms:Genetic Diseases, X-Linked
Hyper-IgM Immunodeficiency Syndrome
Description
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.Search for this term in our Faculty Database
View this term at the NCBI website
