Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Lung disease, immunodeficiency, and chromosome breakage syndrome, 617241, Severe lung disease (possibly viral), thymic hypoplasia, Chromosomal breakage, radiation sensitivity, Combined immunodeficiencies with associated or syndromic features |