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. 2020 Aug 10;22(12):2060–2070. doi: 10.1038/s41436-020-0923-1

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© The Author(s) 2020

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — Associations between genetic etiologies and specific phenotypic terms differ over time, including the association with SCN1A and “Status epilepticus” (HP:0002133, red, a, b), PURA and “Severe Intellectual Disability” (HP:0010864, blue, a, c), and STXBP1 and “Infantile spasms” (HP:0012469, green, a, d). (a) Distribution of the strength of the association over time. (b–d) Frequency of the specific HPO terms in patients with and without the genetic etiology over time that give rise to the observed associations.