Genomics England
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Panels
Genes and Entities
NUDCD3
NudC domain containing 3
OMIM:
610296
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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 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
severe combined immunodeficiency, MONDO:0015974, Omenn syndrome, MONDO:0011338