BCL11B

B-cell CLL/lymphoma 11B
OMIM: 606558
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Intellectual disability, Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities, 618092