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An online compendium of treatable genetic disorders.
Bick, David; Bick, Sarah L; Dimmock, David P; Fowler, Tom A; Caulfield, Mark J; Scott, Richard H.
Affiliation
  • Bick D; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Bick SL; Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
  • Dimmock DP; Rady Children's Institute for Genomic Medicine, San Diego, California, USA.
  • Fowler TA; Genomics England Ltd., London, UK.
  • Caulfield MJ; William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Scott RH; Genomics England Ltd., London, UK.
Am J Med Genet C Semin Med Genet ; 187(1): 48-54, 2021 03.
Article in En | MEDLINE | ID: mdl-33350578
ABSTRACT
More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be challenging to find information concerning treatment for rare diseases as key details are scattered across a number of authoritative websites and numerous journal articles. The website and associated mobile device application described in this article begin to address this challenge by providing a convenient, readily available starting point to find treatment information. The site, Rx-genes.com (https//www.rx-genes.com/), is focused on those conditions where the treatment is directed against the mechanism of the disease and thereby alters the natural history of the disease. The website currently contains 633 disease entries that include references to disease information and treatment guidance, a brief summary of treatments, the inheritance pattern, a disease frequency (if known), nonmolecular confirmatory testing (if available), and a link to experimental treatments. Existing entries are continuously updated, and new entries are added as novel treatments appear in the literature.
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Full text: 1 Database: MEDLINE Main subject: Rare Diseases / Inheritance Patterns Type of study: Guideline Limits: Humans Language: En Journal: Am J Med Genet C Semin Med Genet Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Rare Diseases / Inheritance Patterns Type of study: Guideline Limits: Humans Language: En Journal: Am J Med Genet C Semin Med Genet Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: United States