Genomics England
GMS Panels
Panels
Genes and Entities
RBL2
RB transcriptional corepressor like 2
OMIM:
180203
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Panel
Mode of inheritance
Details
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Intellectual disability
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