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. 2024 Oct 29;16:125. doi: 10.1186/s13073-024-01390-9

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Venn diagram of genes associated with paediatric cardiomyopathy. Literature—genes identified in paediatric cardiomyopathy studies and case reports; PanelApp R135 green—genes on R135 paediatric or syndromic cardiomyopathy PanelApp panel v3.44 with the highest level of evidence; PanelApp Version 1—genes on the original versions of hypertrophic, dilated, left ventricular non-compaction and arrhythmogenic cardiomyopathy panels most likely applied to those recruited to 100,000 Genomes Project in 2015–2018; Other Panels—genes on 6 other paediatric cardiomyopathy panels including Invitae, GeneDx, Ambry, Laboratory for Molecular Medicine, PanelApp Australia and Amsterdam Genetics. See Additional file 1: Tables S1–S4 for full gene lists