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Resource ValueSet/FHIR Server from package ihe.pcc.aps#current (32 ms)

Package ihe.pcc.aps
Type ValueSet
Id Id
FHIR Version R4
Source https://profiles.ihe.net/PCC/APS/https://build.fhir.org/ig/IHE/PCC.APS/ValueSet-Antepartum.Family.History.and.Genetic.Screening.VS.html
Url https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS
Version 0.0.1-current
Status draft
Date 2023-10-24T22:43:25+00:00
Name Antepartum_Family_History_and_Genetic_Screening_VS
Title Antepartum Family History and Genetic Screening
Experimental False
Realm uv
Authority ihe
Description TBD

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct SNOMED codes used in this IG
http://snomed.info/sct SNOMED CT Canada Immunizations


Narrative

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


Source

{
  "resourceType" : "ValueSet",
  "id" : "Antepartum.Family.History.and.Genetic.Screening.VS",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/408856003\">408856003</a></td><td>Autism</td></tr><tr><td><a href=\"http://snomed.info/id/414022008\">414022008</a></td><td>Blood Disorders</td></tr><tr><td><a href=\"http://snomed.info/id/80544005\">80544005</a></td><td>Canavan Disease</td></tr><tr><td><a href=\"http://snomed.info/id/409709004\">409709004</a></td><td>Chromosomal Disorder Includes any inherited genetic or chromosomal disorders</td></tr><tr><td><a href=\"http://snomed.info/id/13213009\">13213009</a></td><td>Congenital Heart Defect</td></tr><tr><td><a href=\"http://snomed.info/id/190905008\">190905008</a></td><td>Cystic Fibrosis</td></tr><tr><td><a href=\"http://snomed.info/id/276720006\">276720006</a></td><td>Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects</td></tr><tr><td><a href=\"http://snomed.info/id/41040004\">41040004</a></td><td>Down Syndrome</td></tr><tr><td><a href=\"http://snomed.info/id/29159009\">29159009</a></td><td>Familial Dysautonomia</td></tr><tr><td><a href=\"http://snomed.info/id/90935002\">90935002</a></td><td>Hemophilia</td></tr><tr><td><a href=\"http://snomed.info/id/58756001\">58756001</a></td><td>Huntington's Chorea</td></tr><tr><td><a href=\"http://snomed.info/id/75934005\">75934005</a></td><td>Maternal Metabolic Disorder</td></tr><tr><td><a href=\"http://snomed.info/id/91138005\">91138005</a></td><td>Mental Retardation</td></tr><tr><td><a href=\"http://snomed.info/id/73297009\">73297009</a></td><td>Muscular Dystrophy</td></tr><tr><td><a href=\"http://snomed.info/id/253098009\">253098009</a></td><td>Neural Tube Defect</td></tr><tr><td><a href=\"http://snomed.info/id/102878001\">102878001</a></td><td>Recurrent pregnancy loss/stillbirth</td></tr><tr><td><a href=\"http://snomed.info/id/417357006\">417357006</a></td><td>Sickle Cell Disease</td></tr><tr><td><a href=\"http://snomed.info/id/16402000\">16402000</a></td><td>Sickle Cell Trait</td></tr><tr><td><a href=\"http://snomed.info/id/111385000\">111385000</a></td><td>Tay-Sachs</td></tr><tr><td><a href=\"http://snomed.info/id/40108008\">40108008</a></td><td>Thalassemia</td></tr></table></li></ul></div>"
  },
  "url" : "https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS",
  "version" : "0.0.1-current",
  "name" : "Antepartum_Family_History_and_Genetic_Screening_VS",
  "title" : "Antepartum Family History and Genetic Screening",
  "status" : "draft",
  "experimental" : false,
  "date" : "2023-10-24T22:43:25+00:00",
  "publisher" : "IHE Patient Care Coordination Committee",
  "contact" : [
    {
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.ihe.net/ihe_domains/patient_care_coordination/"
        }
      ]
    },
    {
      "telecom" : [
        {
          "system" : "email",
          "value" : "pcc@ihe.net"
        }
      ]
    },
    {
      "name" : "IHE Patient Care Coordination Committee",
      "telecom" : [
        {
          "system" : "email",
          "value" : "pcc@ihe.net"
        }
      ]
    }
  ],
  "description" : "TBD",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001"
        }
      ]
    }
  ],
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "408856003",
            "display" : "Autism"
          },
          {
            "code" : "414022008",
            "display" : "Blood Disorders"
          },
          {
            "code" : "80544005",
            "display" : "Canavan Disease"
          },
          {
            "code" : "409709004",
            "display" : "Chromosomal Disorder Includes any inherited genetic or chromosomal disorders"
          },
          {
            "code" : "13213009",
            "display" : "Congenital Heart Defect"
          },
          {
            "code" : "190905008",
            "display" : "Cystic Fibrosis"
          },
          {
            "code" : "276720006",
            "display" : "Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects"
          },
          {
            "code" : "41040004",
            "display" : "Down Syndrome"
          },
          {
            "code" : "29159009",
            "display" : "Familial Dysautonomia"
          },
          {
            "code" : "90935002",
            "display" : "Hemophilia"
          },
          {
            "code" : "58756001",
            "display" : "Huntington's Chorea"
          },
          {
            "code" : "75934005",
            "display" : "Maternal Metabolic Disorder"
          },
          {
            "code" : "91138005",
            "display" : "Mental Retardation"
          },
          {
            "code" : "73297009",
            "display" : "Muscular Dystrophy"
          },
          {
            "code" : "253098009",
            "display" : "Neural Tube Defect"
          },
          {
            "code" : "102878001",
            "display" : "Recurrent pregnancy loss/stillbirth"
          },
          {
            "code" : "417357006",
            "display" : "Sickle Cell Disease"
          },
          {
            "code" : "16402000",
            "display" : "Sickle Cell Trait"
          },
          {
            "code" : "111385000",
            "display" : "Tay-Sachs"
          },
          {
            "code" : "40108008",
            "display" : "Thalassemia"
          }
        ]
      }
    ]
  }
}

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