Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 6.12 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Recurrent infections, facial dysmorphism, limb anomalies, Predominantly Antibody Deficiencies, Hoffman syndrome/TOP2B deficiency |