CNTN2

Panel	Reviews	Mode of inheritance	Details
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Green CNTN2 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Epilepsy, MONDO:0015653, CNTN2-related
Green CNTN2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Epilepsy, MONDO:0015653, CNTN2-related Epilepsy, myoclonic, familial adult, 5 MIM#615400
Amber CNTN2 in Familial Generalised Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 0.14	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber GREP Literature Phenotypes Epilepsy, familial adult myoclonic, 5

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