Genomics England
GMS Panels
Panels
Genes and Entities
ISCA-46292-Loss
22q11.2 recurrent region (distal type III, D-G/H) (includes SMARCB1) Loss
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Panel
Mode of inheritance
Details
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Intellectual disability
Component of the following Super Panels:
- Childhood onset leukodystrophy
- Hypotonic infant
- Paediatric disorders
R-numbers:
R29
Signed-off version 6.13
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes