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Early onset or syndromic epilepsy v1.191 | CNTNAP2 | Rebecca Foulger Source Wessex and West Midlands GLH was added to CNTNAP2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.190 | CNTNAP2 | Rebecca Foulger Source NHS GMS was added to CNTNAP2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.189 | CNTNAP2 | Rebecca Foulger reviewed gene: CNTNAP2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy v1.188 | CNTNAP2 | Tracy Lester reviewed gene: CNTNAP2: Rating: GREEN; Mode of pathogenicity: ; Publications: 16571880, 18179893, 27439707 ; Phenotypes: Cortical dysplasia-focal epilepsy syndrome,610042, Pitt-Hopkins like syndrome 1,610042, {Autism susceptibility 15},612100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Early onset or syndromic epilepsy | CNTNAP2 | Sarah Leigh Added gene to panel |