AICDA

activation induced cytidine deaminase
OMIM: 605257
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Immunodeficiency with hyper-IgM, type 2, Hyper IgM syndrome with lymphoid hyperplasia, Immunodeficiency with hyper-IgM, type 2, 605258, Primary Immune Deficiencies, CSR defects and Hyper IgM (HIGM) syndromes, Bacterial infections, enlarged lymph nodes and germinal centers, Predominantly Antibody Deficiencies