{
  "package" : "hl7.terminology@6.3.0",
  "definition" : "Global Rare Disease Patient Registry and Data Repository (GRDR) consent is an agreement of a healthcare consumer to permit collection, access, use and disclosure of de-identified rare disease information and collection of bio-specimens, medical information, family history and other related information from patients to permit the registry collection of health and genetic information, and specimens for pseudonymized disclosure for research purpose of use. https://rarediseases.info.nih.gov/files/informed_consent_template.pdf",
  "system" : "http://terminology.hl7.org/CodeSystem/consentpolicycodes",
  "property" : [ ],
  "codesystem" : "f9f54872-8956-58a8-97c0-12545febcf80",
  "concept_id" : "51436d66-fa36-5eb0-8d70-c631ea7cf651",
  "ancestors" : {
    "nih-grdr" : 0
  },
  "id" : "751aec2c-d8ef-4909-808b-0ab3f8eca390",
  "code" : "nih-grdr",
  "display" : "NIH Global Rare Disease Patient Registry and Data Repository consent",
  "version" : "3.0.1"
}