TOP2B

DNA topoisomerase II beta
OMIM: 126431
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 3.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Recurrent infections, facial dysmorphism, limb anomalies, Predominantly Antibody Deficiencies, Hoffman syndrome/TOP2B deficiency