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

Packageihe.pcc.maps
TypeValueSet
IdAntepartum.Family.History.and.Genetic.Screening.VS
FHIR VersionR4
Sourcehttps://profiles.ihe.net/PCC/mAPS/https://build.fhir.org/ig/IHE/PCC.mAPS/ValueSet-Antepartum.Family.History.and.Genetic.Screening.VS.html
URLhttps://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS
Version1.0.0
Statusactive
Date2024-10-29T20:32:09+00:00
NameAntepartum_Family_History_and_Genetic_Screening_VS
TitleAntepartum Family History and Genetic Screening
Realmuv
Authorityihe
DescriptionThis value set includes the type of genetic-related risks identified through screening of the patient’s and biological father’s family history.

Resources that use this resource

StructureDefinition
IHE.Antepartum.Genetic.ScreeningAntepartum Genetic Screenings

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

Generated Narrative: ValueSet Antepartum.Family.History.and.Genetic.Screening.VS


Source

{
  "resourceType": "ValueSet",
  "id": "Antepartum.Family.History.and.Genetic.Screening.VS",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "url": "https://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS",
  "version": "1.0.0",
  "name": "Antepartum_Family_History_and_Genetic_Screening_VS",
  "title": "Antepartum Family History and Genetic Screening",
  "status": "active",
  "experimental": false,
  "date": "2024-10-29T20:32:09+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": "This value set includes the type of genetic-related risks identified through screening of the patient’s and biological father’s family history.",
  "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"
          }
        ]
      }
    ]
  }
}