BR serine/threonine kinase 2
OMIM: 609236
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Global developmental delay, Autism, Behavioral abnormality, Global developmental delay, Intellectual disability, Autism, Behavioral abnormality, Intellectual disability