Panel | Mode of inheritance | Details |
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1 panel | ||
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Absence epilepsy, Cerebellar atrophy with seizures and variable developmental delay, 618501 |