RBL2

RB transcriptional corepressor like 2
OMIM: 180203
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Brunet-Wagner neurodevelopmental syndrome, OMIM:619690