FHIR IG analytics

Resources that use this resource

Resources that this resource uses

Narrative

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

Source1

{
  "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": "2026-02-03T22:52:22+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": "Disorder of cellular component of blood"
          },
          {
            "code": "80544005",
            "display": "Spongy degeneration of central nervous system"
          },
          {
            "code": "409709004",
            "display": "Chromosomal disorder"
          },
          {
            "code": "13213009",
            "display": "Congenital heart disease"
          },
          {
            "code": "190905008",
            "display": "Cystic Fibrosis"
          },
          {
            "code": "276720006",
            "display": "Dysmorphism"
          },
          {
            "code": "41040004",
            "display": "Down Syndrome"
          },
          {
            "code": "29159009",
            "display": "Familial Dysautonomia"
          },
          {
            "code": "90935002",
            "display": "Hemophilia"
          },
          {
            "code": "58756001",
            "display": "Huntington's Chorea"
          },
          {
            "code": "75934005",
            "display": "Metabolic disease"
          },
          {
            "code": "91138005",
            "display": "Mental Retardation"
          },
          {
            "code": "73297009",
            "display": "Muscular Dystrophy"
          },
          {
            "code": "253098009",
            "display": "Neural Tube Defect"
          },
          {
            "code": "102878001",
            "display": "Recurrent abortion"
          },
          {
            "code": "417357006",
            "display": "Sickle Cell Disease"
          },
          {
            "code": "16402000",
            "display": "Sickle Cell Trait"
          },
          {
            "code": "111385000",
            "display": "Tay-Sachs disease"
          },
          {
            "code": "40108008",
            "display": "Thalassemia"
          }
        ]
      }
    ]
  }
}