Genomics England
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Panels
Genes and Entities
AICDA
activation induced cytidine deaminase
OMIM:
605257
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Panel
Mode of inheritance
Details
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Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers:
R15
Signed-off version 5.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Immunodeficiency with hyper-IgM, type 2, OMIM:605258