CSNK2B

casein kinase 2 beta
OMIM: 115441
PanelMode of inheritanceDetails
2 panels
R-numbers: R59
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732, Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732, Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889