Genomics England
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Panels
Genes and Entities
CR2
complement C3d receptor 2
OMIM:
120650
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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
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Immunodeficiency, common variable, 7, OMIM:614699