Genomics England
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Genes and Entities
C2
complement C2
OMIM:
613927
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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 9.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
C2 deficiency, OMIM:217000, complement component 2 deficiency, MONDO:0009006