<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>OD</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA753890</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>As the COVID-19 pandemic evolved in early 2020, case reports appeared describing children with unusual febrile illnesses with elevated inflammatory markers and multi-system involvement that is now termed Multisystem Inflammatory Syndrome in Children (MIS-C). The illness occurs weeks following exposure to SARS-CoV-2 and these children have a wide spectrum of disease severity, ranging from cardiogenic shock to milder illness that can be self-limited. To address an urgent, unmet clinical need, investigative teams across three countries will join forces to discover and validate a diagnostic test to identify children with MIS-C and predict progression of disease.The emergence of MIS-C is so new and so rapidly evolving that there are currently no diagnostic tests to identify these patients,... (for more see dbGaP study page.)</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Rapid Acceleration of Diagnostics - Radical (RADx-rad): Characterization of Multisystem Inflammatory Syndrome in Children and its Relationship to Kawasaki Disease</name><description>Rapid Acceleration of Diagnostics - Radical (RADx-rad): Characterization of Multisystem Inflammatory Syndrome in Children and its Relationship to Kawasaki Disease</description><dates><last_updated>2025-09-24</last_updated><first_public>2022-11-24</first_public></dates><accession>PRJNA753890</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>