AICDA

activation induced cytidine deaminase
OMIM: 605257
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 6.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Immunodeficiency with hyper-IgM, type 2, OMIM:605258