ISCA-37392-Gain

7q11.23 recurrent (Williams-Beuren syndrome) region (includes ELN) Gain
PanelMode of inheritanceDetails
1 panel
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
intellectual disability, 609757, behavior problems, abnormal gait and station, cardiovascular disease, phonologic disorders, distinctive facial features, neurologic abnormalities, speech sound disorders