Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 6.9 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Global developmental delay, Intellectual disability, Seizures, Cerebral white matter atrophy, Abnormality of the corpus callosum, Abnormality of movement, Stereotypic behavior, Abnormality of head or neck, Short foot |
Green in Severe microcephalyR-numbers: R88 Signed-off version 6.8 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Global developmental delay, Intellectual disability, Seizures, Cerebral white matter atrophy, Abnormality of the corpus callosum, Abnormality of movement, Stereotypic behavior, Abnormality of head or neck, Short foot |