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(616516)","Emery-Dreifuss muscular dystrophy 2, autosomal dominant (181350)","Cardiomyopathy, dilated, 1A (115200)","Cardiomyopathy, dilated, 1A","Lipodystrophy, familial partial, type 2 (151660)","Emery-Dreifuss muscular dystrophy 2, AD, 181350","Mandibuloacral dysplasia (248370)","Malouf syndrome (212112)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":750,"hash_id":null,"name":"Sudden cardiac death","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-09-24T10:05:54.784946Z","relevant_disorders":["Molecular autopsy","R138"],"stats":{"number_of_genes":119,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}