This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
|Medical Terms||Other Names||
|Percent of people who have these symptoms is not available through HPO|
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Got a Great Research Idea? ‘All of Us’ Wants to Hear It!
January 18, 2018
New NCATS Rare Diseases Research Video
December 27, 2017
Rare Disease Day at NIH on March 1, 2018
December 19, 2017
Workshop on Harmonization of EBV Testing for Nasopharyngeal Cancer
Monday, November 16, 2015 -
Thursday, November 17, 2016
Location: Bethesda, MD
Description: The National Cancer Institute (NCI) is convening a workshop on the harmonization of EBV testing that might have clinical utility in treatment decision-making for advanced nasopharyngeal cancer. The purpose of the workshop is to bring together experts in assay development, clinical laboratory directors, and head and neck oncologists to assess the need for harmonization of EBV testing, identify best approaches to establish harmonization, and explore ways to effect widespread adoption of harmonized assay procedures and references.
Contact: Dr. Kelly Kim240email@example.com
Co-funding Institute(s): National Cancer Institute, Office of Rare Diseases Research
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