Id2.16.840.1.113883.10.20.20.1.9.1Effective Date2013‑02‑01
Statusdraft DraftVersion Label
NameBackgroundSectionDisplay NameBackground Section
Description
The Background Section nests within the TestInformationSection and its text attribute consists of narrative describing background of the genetic test at stake. Future releases of standard may suggest templates for structured data representing background information.
ContextParent nodes of template element with id 2.16.840.1.113883.10.20.20.1.9.1
ClassificationCDA Section Level Template
Open/ClosedOpen (other than defined elements are allowed)
Used by / Uses
Used by 1 transaction and 4 templates, Uses 0 templates
Used by as NameVersion
2.16.840.1.113883.3.1937.777.20.4.2Transactiondraft Genetic Testing Report (GTR) (DSTU Release 1)2018‑03‑22 11:37:04
2.16.840.1.113883.2.6.60.13.10.19Containmentdraft Testinformationen Section2018‑10‑25 13:45:32
2.16.840.1.113883.10.20.20linkdraft Genetic Testing Report2013‑02‑01
2.16.840.1.113883.10.20.20.1.8linkdraft Test Details Section2013‑02‑01
2.16.840.1.113883.10.20.20.1.9Containmentdraft Test Information Section2013‑02‑01
RelationshipSpecialization: template 2.16.840.1.113883.10.12.201 CDA Section (2005‑09‑07)
ref
ad1bbr-
Example
Example
<section>
  <templateId root="2.16.840.1.113883.10.20.20.1.9.1"/>  <title>Background</title>  <text>
    <list>
      <item>
        <content>
Mutations in the GJB2 (connexin 26) gene are the most common cause of
non syndromic hearing loss and are most often seen in a person with
hearing loss that was found in early childhood without any other medical
problems. The severity of the hearing loss can range from mild to profound.
The inheritance pattern is usually autosomal recessive, requiring two
mutations, one in each copy of the gene, to cause hearing loss. The GJB6-
D13S1830 deletion removes most of the GJB6 gene, which encodes the connexin
30 protein (Cx30). This deletion, when present in two copies or when
combined with a single connexin 26 mutation, causes hearing loss. Although
the frequency of mitochondrial hearing loss is unknown, studies suggest
that mitochondrial mutations play an important role in inherited and
acquired hearing impairment.
</content>      </item>    </list>  </text></section>
ItemDTCardConfDescriptionLabel
hl7:section
Backdotstion
hl7:templateId
II1 … 1MBackdotstion
@root
uid1 … 1F2.16.840.1.113883.10.20.20.1.9.1
hl7:code
0 … 1RBackdotstion
 ConstraintGtr Background Section MAY contain a code that represents background information supporting the general description of the performed genetic test, e.g., LOINC code 35511-5, "Background information section".
hl7:title
1 … 1RBackdotstion
 ConstraintTitle SHALL contain text that implies "Background information supporting the general description of the performed genetic test(s)"