...
首页> 外文期刊>American journal of medical genetics, Part A >Human disease genes website series: An international, open and dynamic library for up-to-date clinical information
【24h】

Human disease genes website series: An international, open and dynamic library for up-to-date clinical information

机译:人类疾病基因网站系列:用于最新临床信息的国际,开放和动态库

获取原文
获取原文并翻译 | 示例
           

摘要

Since the introduction of next-generation sequencing, an increasing number of disorders have been discovered to have genetic etiology. To address diverse clinical questions and coordinate research activities that arise with the identification of these rare disorders, we developed the Human Disease Genes website series (HDG website series): an international digital library that records detailed information on the clinical phenotype of novel genetic variants in the human genome (https://humandiseasegenes.info/). Each gene website is moderated by a dedicated team of clinicians and researchers, focused on specific genes, and provides up-to-date-including unpublished-clinical information. The HDG website series is expanding rapidly with 424 genes currently adopted by 325 moderators from across the globe. On average, a gene website has detailed phenotypic information of 14.4 patients. There are multiple examples of added value, one being the ARID1B gene website, which was recently utilized in research to collect clinical information of 81 new patients. Additionally, several gene websites have more data available than currently published in the literature. In conclusion, the HDG website series provides an easily accessible, open and up-to-date clinical data resource for patients with pathogenic variants of individual genes. This is a valuable resource not only for clinicians dealing with rare genetic disorders such as developmental delay and autism, but other professionals working in diagnostics and basic research. Since the HDG website series is a dynamic platform, its data also include the phenotype of yet unpublished patients curated by professionals providing higher quality clinical detail to improve management of these rare disorders.
机译:None

著录项

  • 来源
  • 作者单位

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

    Univ Washington Sch Med Dept Genome Sci Seattle WA USA;

    Univ Adelaide Adelaide Med Sch Adelaide SA Australia;

    Radboud Univ Nijmegen Med Ctr Donders Inst Brain Cognit &

    Behav Dept Human Genet POB 9101 NL;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学遗传学;
  • 关键词

    clinical data; HDG; HDG website series; HPO; online resource; phenotype;

    机译:临床数据;HDG;HDG网站系列;HPO;在线资源;表型;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号