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Resource NamingSystem/FHIR Server from package hl7.terminology#current (31 ms)

Package hl7.terminology
Type NamingSystem
Id Id
FHIR Version R5
Source http://terminology.hl7.org/https://build.fhir.org/ig/HL7/UTG/NamingSystem-ISCN.html
Url http://terminology.hl7.org/NamingSystem/ISCN
Version 1.0.1
Status active
Date 2022-06-07T00:00:00-00:00
Name ISCN
Title International System for Human Cytogenomic Nomenclature (ISCN)
Experimental False
Realm uv
Authority hl7
Description The International System for Human Cytogenetic Nomenclature (ISCN) was created by the International Standing committee on Human Cytogenetic Nomenclature to represent the outcome of cytogenetic tests. ISCN specifies the nomenclature to describe karyotypes, chromosome abnormalities, in situ hybridization, etc. ISCN provides a list of symbols and abbreviated terms in adjunction with a set of rules, which can be used in the description of chromosomes and chromosome abnormalities, such as p for short arm of chromosome, q for long arm of chromosome, cen for centromere, del for deletion, ish for in situ hybridization, and plus sign (+) for gain, etc. A LOINC code is created to represent "chromosome analysis results in ISCN expression". In HL7 v2 messages, this LOINC code is used in OBX-3 with a coded result (CWE data type) that will be sent in OBX-5. The value of the coded result is an ISCN expression, and ISCN will be the code system for the coded result.
Kind codesystem

Resources that use this resource

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Resources that this resource uses

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: NamingSystem ISCN

Summary

Defining URLhttp://terminology.hl7.org/NamingSystem/ISCN
Version1.0.1
NameISCN
TitleInternational System for Human Cytogenomic Nomenclature (ISCN)
Statusactive
Definition

The International System for Human Cytogenetic Nomenclature (ISCN) was created by the International Standing committee on Human Cytogenetic Nomenclature to represent the outcome of cytogenetic tests. ISCN specifies the nomenclature to describe karyotypes, chromosome abnormalities, in situ hybridization, etc. ISCN provides a list of symbols and abbreviated terms in adjunction with a set of rules, which can be used in the description of chromosomes and chromosome abnormalities, such as p for short arm of chromosome, q for long arm of chromosome, cen for centromere, del for deletion, ish for in situ hybridization, and plus sign (+) for gain, etc.

A LOINC code is created to represent "chromosome analysis results in ISCN expression". In HL7 v2 messages, this LOINC code is used in OBX-3 with a coded result (CWE data type) that will be sent in OBX-5. The value of the coded result is an ISCN expression, and ISCN will be the code system for the coded result.

PublisherS. Karger AG

Identifiers

TypeValuePreferredPeriodComment
OID2.16.840.1.113883.6.299true
URIhttps://iscn.karger.comtrue2021-01-27 --> (ongoing)Official canonical URL going forward.

Source

{
  "resourceType" : "NamingSystem",
  "id" : "ISCN",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: NamingSystem ISCN</b></p><a name=\"ISCN\"> </a><a name=\"hcISCN\"> </a><a name=\"ISCN-en-US\"> </a><h3>Summary</h3><table class=\"grid\"><tr><td>Defining URL</td><td>http://terminology.hl7.org/NamingSystem/ISCN</td></tr><tr><td>Version</td><td>1.0.1</td></tr><tr><td>Name</td><td>ISCN</td></tr><tr><td>Title</td><td>International System for Human Cytogenomic Nomenclature (ISCN)</td></tr><tr><td>Status</td><td>active</td></tr><tr><td>Definition</td><td><div><p>The International System for Human Cytogenetic Nomenclature (ISCN) was created by the International Standing committee on Human Cytogenetic Nomenclature to represent the outcome of cytogenetic tests. ISCN specifies the nomenclature to describe karyotypes, chromosome abnormalities, in situ hybridization, etc. ISCN provides a list of symbols and abbreviated terms in adjunction with a set of rules, which can be used in the description of chromosomes and chromosome abnormalities, such as p for short arm of chromosome, q for long arm of chromosome, cen for centromere, del for deletion, ish for in situ hybridization, and plus sign (+) for gain, etc.</p>\n<p>A LOINC code is created to represent &quot;chromosome analysis results in ISCN expression&quot;. In HL7 v2 messages, this LOINC code is used in OBX-3 with a coded result (CWE data type) that will be sent in OBX-5. The value of the coded result is an ISCN expression, and ISCN will be the code system for the coded result.</p>\n</div></td></tr><tr><td>Publisher</td><td>S. Karger AG</td></tr></table><h3>Identifiers</h3><table class=\"grid\"><tr><td><b>Type</b></td><td><b>Value</b></td><td><b>Preferred</b></td><td><b>Period</b></td><td><b>Comment</b></td></tr><tr><td>OID</td><td>2.16.840.1.113883.6.299</td><td>true</td><td></td><td/></tr><tr><td>URI</td><td>https://iscn.karger.com</td><td>true</td><td>2021-01-27 --&gt; (ongoing)</td><td>Official canonical URL going forward.</td></tr></table></div>"
  },
  "url" : "http://terminology.hl7.org/NamingSystem/ISCN",
  "version" : "1.0.1",
  "name" : "ISCN",
  "title" : "International System for Human Cytogenomic Nomenclature (ISCN)",
  "status" : "active",
  "kind" : "codesystem",
  "date" : "2022-06-07T00:00:00-00:00",
  "publisher" : "S. Karger AG",
  "contact" : [
    {
      "name" : "S. Karger AG; P.O Box, CH-4009 Basel (Switzerland) Allschwilerstrasse 10, CH-4055 Basel",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.karger.com/"
        },
        {
          "system" : "email",
          "value" : "info@signaturegenomics.com"
        },
        {
          "system" : "phone",
          "value" : "+41 61 306 11 11"
        }
      ]
    }
  ],
  "description" : "The International System for Human Cytogenetic Nomenclature (ISCN) was created by the International Standing committee on Human Cytogenetic Nomenclature to represent the outcome of cytogenetic tests. ISCN specifies the nomenclature to describe karyotypes, chromosome abnormalities, in situ hybridization, etc. ISCN provides a list of symbols and abbreviated terms in adjunction with a set of rules, which can be used in the description of chromosomes and chromosome abnormalities, such as p for short arm of chromosome, q for long arm of chromosome, cen for centromere, del for deletion, ish for in situ hybridization, and plus sign (+) for gain, etc.\r\n\r\nA LOINC code is created to represent \"chromosome analysis results in ISCN expression\". In HL7 v2 messages, this LOINC code is used in OBX-3 with a coded result (CWE data type) that will be sent in OBX-5. The value of the coded result is an ISCN expression, and ISCN will be the code system for the coded result.",
  "uniqueId" : [
    {
      "type" : "oid",
      "value" : "2.16.840.1.113883.6.299",
      "preferred" : true
    },
    {
      "type" : "uri",
      "value" : "https://iscn.karger.com",
      "preferred" : true,
      "comment" : "Official canonical URL going forward.",
      "period" : {
        "start" : "2021-01-27"
      }
    }
  ]
}

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