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FHIR IG Statistics: ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS

Packageihe.pcc.aps
TypeValueSet
IdAntepartum.Family.History.and.Genetic.Screening.VS
FHIR VersionR4
Sourcehttps://profiles.ihe.net/PCC/APS/https://build.fhir.org/ig/IHE/PCC.APS/ValueSet-Antepartum.Family.History.and.Genetic.Screening.VS.html
URLhttps://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS
Version0.0.1-current
Statusdraft
Date2023-10-24T22:43:25+00:00
NameAntepartum_Family_History_and_Genetic_Screening_VS
TitleAntepartum Family History and Genetic Screening
Realmuv
Authorityihe
DescriptionTBD

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)
sctSNOMED codes used in this IG
sctveri

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": "<!-- snip (see above) -->"
  },
  "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"
          }
        ]
      }
    ]
  }
}