Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R15 Signed-off version 6.12 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Immunodeficiency, common variable, 12 616576, Common variable immunodeficiency disorders (CVID), Unclassified antibody deficiency, Recurrent sinopulmonary infections, COPD, EBV proliferation, autoimmune cytopenias, alopecia and autoimmune thyroiditis, Predominantly Antibody Deficiencies |
R-numbers: R189 Signed-off version 3.10 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Immunodeficiency, common variable, 12, 616576, Recurrent sinopulmonary infections |