Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R15 Signed-off version 7.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Immunodeficiency 14A, autosomal dominant, OMIM:615513, Immunodeficiency 14B, autosomal recessive, OMIM:619281, Combined immunodeficiency, Activated PI3K-delta syndrome (APDS), Predominantly Antibody Deficiencies, Sinopulmonary infections, dysgammaglobulinaemia, lymphadenopathy, nodular lymphoid hyperplasia and herpesviremia, Severe bacterial infections |
R-numbers: R189 Signed-off version 3.10 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Immunodeficiency 14A, autosomal dominant, OMIM:615513, Bronchiectasis |