FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.4.11  |  FHIR Version n/a  User: [n/a]

Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (109 ms)

Package us.nlm.vsac
Type ValueSet
Id Id
FHIR Version R4
Source http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.464.1003.120.12.1007/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.12.1007
Version 20170504
Status active
Date 2022-03-07T11:14:02-05:00
Name SevereCombinedImmunodeficiency
Title Severe Combined Immunodeficiency
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of severe combined immunodeficiency including both genetic and other causes.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of a severe combined immunodeficiency including genetic conditions and other causes.),(Exclusion Criteria: No exclusions.)

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1011 Severe Combined Immunodeficiency
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1012 Severe Combined Immunodeficiency


Source

{
  "resourceType" : "ValueSet",
  "id" : "2.16.840.1.113883.3.464.1003.120.12.1007",
  "meta" : {
    "versionId" : "5",
    "lastUpdated" : "2023-12-21T17:43:03.000-05:00",
    "profile" : [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
    ]
  },
  "extension" : [
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-author",
      "valueContactDetail" : {
        "name" : "NCQA PHEMUR Author"
      }
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-02-14"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2017-05-04"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.12.1007",
  "identifier" : [
    {
      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113883.3.464.1003.120.12.1007"
    }
  ],
  "version" : "20170504",
  "name" : "SevereCombinedImmunodeficiency",
  "title" : "Severe Combined Immunodeficiency",
  "status" : "active",
  "experimental" : false,
  "date" : "2022-03-07T11:14:02-05:00",
  "publisher" : "NCQA PHEMUR",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US"
        }
      ]
    }
  ],
  "purpose" : "(Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of severe combined immunodeficiency including both genetic and other causes.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of a severe combined immunodeficiency including genetic conditions and other causes.),(Exclusion Criteria: No exclusions.)",
  "compose" : {
    "include" : [
      {
        "valueSet" : [
          "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1012"
        ]
      },
      {
        "valueSet" : [
          "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1011"
        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:011b1544-5096-4b10-a0f6-4479637e341a",
    "timestamp" : "2024-12-10T10:45:04-05:00",
    "total" : 51,
    "contains" : [
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "111584000",
        "display" : "Reticular dysgenesis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "111587007",
        "display" : "Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1179284005",
        "display" : "Severe combined immunodeficiency due to linker for activation of T cells deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1229940001",
        "display" : "Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1229941002",
        "display" : "Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1229942009",
        "display" : "Severe combined immunodeficiency due to coronin 1A deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "190996002",
        "display" : "Severe combined immunodeficiency with reticular dysgenesis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "190997006",
        "display" : "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "190998001",
        "display" : "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "191001007",
        "display" : "Major histocompatibility complex class I deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "191002000",
        "display" : "Major histocompatibility complex class II deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "22406001",
        "display" : "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "234570002",
        "display" : "Severe combined immunodeficiency with maternofetal engraftment (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "234571003",
        "display" : "Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "31323000",
        "display" : "Severe combined immunodeficiency disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "3439009",
        "display" : "Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "350353007",
        "display" : "De Vaal's syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "351287008",
        "display" : "Reticular dysgenesis with congenital aleukocytosis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "362993009",
        "display" : "Autosomal recessive severe combined immunodeficiency disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "36980009",
        "display" : "Severe combined immunodeficiency due to absent adenosine deaminase (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "44940001",
        "display" : "Adenosine deaminase deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "45390000",
        "display" : "Severe combined immunodeficiency due to absent interleukin-2 production (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "49555001",
        "display" : "Severe combined immunodeficiency due to absent T cell receptor (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "55602000",
        "display" : "Nezelof's syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "715982006",
        "display" : "Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "716378008",
        "display" : "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "716871006",
        "display" : "Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "718107000",
        "display" : "Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "71904008",
        "display" : "Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "720345008",
        "display" : "Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "720853005",
        "display" : "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "720986005",
        "display" : "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "721977007",
        "display" : "Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "722067005",
        "display" : "Severe combined immunodeficiency with hypereosinophilia (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "724177005",
        "display" : "Ligase 4 syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "724361001",
        "display" : "Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "725135004",
        "display" : "Combined immunodeficiency due to CD3gamma deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "725136003",
        "display" : "Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "725290000",
        "display" : "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "763623001",
        "display" : "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "765145001",
        "display" : "T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "765188009",
        "display" : "Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "771517009",
        "display" : "Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "782751003",
        "display" : "Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "783617001",
        "display" : "Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "789777007",
        "display" : "Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "987840791000119102",
        "display" : "Adenosine deaminase 2 deficiency (disorder)"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "D81.0",
        "display" : "Severe combined immunodeficiency [SCID] with reticular dysgenesis"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "D81.1",
        "display" : "Severe combined immunodeficiency [SCID] with low T- and B-cell numbers"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "D81.2",
        "display" : "Severe combined immunodeficiency [SCID] with low or normal B-cell numbers"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "D81.9",
        "display" : "Combined immunodeficiency, unspecified"
      }
    ]
  },
  "text" : {
  }
}

XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.