Genomics England
GMS Panels
Panels
Genes and Entities
ISCA-37392-Loss
7q11.23 recurrent (Williams-Beuren syndrome) region (includes ELN) Loss
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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
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
194050, Williams syndrome