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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (171 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/2.16.840.1.113883.3.464.1003.120.11.1001/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1001
Version 20240206
Status active
Date 2024-02-06T01:09:28-05:00
Name DisordersOfTheImmuneSystem
Title Disorders of the Immune System
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of conditions affecting the immune system.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of disorders of the immune system including disorders of the immunoglobulins and the complement system.),(Exclusion Criteria: No exclusions.)

Resources that use this resource

ValueSet
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.12.1001 Disorders of the Immune System

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri


Source

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  "meta" : {
    "versionId" : "63",
    "lastUpdated" : "2024-02-06T01:09:28.000-05:00",
    "profile" : [
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      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
    ]
  },
  "extension" : [
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      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-author",
      "valueContactDetail" : {
        "name" : "NCQA PHEMUR Author"
      }
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-02-06"
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      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2024-02-06"
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  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.120.11.1001",
  "identifier" : [
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      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113883.3.464.1003.120.11.1001"
    }
  ],
  "version" : "20240206",
  "name" : "DisordersOfTheImmuneSystem",
  "title" : "Disorders of the Immune System",
  "status" : "active",
  "date" : "2024-02-06T01:09:28-05:00",
  "publisher" : "NCQA PHEMUR",
  "jurisdiction" : [
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  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "1144907001",
            "display" : "Late acute graft-versus-host disease (disorder)"
          },
          {
            "code" : "1144908006",
            "display" : "Late chronic graft-versus-host disease (disorder)"
          },
          {
            "code" : "1144963000",
            "display" : "Acute on chronic graft-versus-host disease (disorder)"
          },
          {
            "code" : "1162263002",
            "display" : "Complement component 8 deficiency (disorder)"
          },
          {
            "code" : "1177120001",
            "display" : "Bronchiolitis obliterans syndrome due to and following allogeneic stem cell transplant (disorder)"
          },
          {
            "code" : "1197361002",
            "display" : "Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder)"
          },
          {
            "code" : "1197362009",
            "display" : "Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease (disorder)"
          },
          {
            "code" : "121121000119106",
            "display" : "Acute graft-versus-host reaction following bone marrow transplant (disorder)"
          },
          {
            "code" : "121131000119109",
            "display" : "Chronic graft versus host disease after transplantation of bone marrow (disorder)"
          },
          {
            "code" : "1268379007",
            "display" : "Graft versus host disease of intestine (disorder)"
          },
          {
            "code" : "1279887007",
            "display" : "Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome (disorder)"
          },
          {
            "code" : "128631000119109",
            "display" : "Chronic graft-versus-host disease following kidney transplant (disorder)"
          },
          {
            "code" : "18827005",
            "display" : "Complement abnormality (disorder)"
          },
          {
            "code" : "190979003",
            "display" : "Selective immunoglobulin A deficiency (disorder)"
          },
          {
            "code" : "190980000",
            "display" : "Selective immunoglobulin M deficiency (disorder)"
          },
          {
            "code" : "190981001",
            "display" : "Selective immunoglobulin G deficiency (disorder)"
          },
          {
            "code" : "190996002",
            "display" : "Severe combined immunodeficiency with reticular dysgenesis (disorder)"
          },
          {
            "code" : "190997006",
            "display" : "Severe combined immunodeficiency with low T- and B-cell numbers (disorder)"
          },
          {
            "code" : "190998001",
            "display" : "Severe combined immunodeficiency with low or normal B-cell numbers (disorder)"
          },
          {
            "code" : "191001007",
            "display" : "Major histocompatibility complex class I deficiency (disorder)"
          },
          {
            "code" : "191002000",
            "display" : "Major histocompatibility complex class II deficiency (disorder)"
          },
          {
            "code" : "191011000",
            "display" : "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)"
          },
          {
            "code" : "191012007",
            "display" : "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)"
          },
          {
            "code" : "191013002",
            "display" : "Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)"
          },
          {
            "code" : "191018006",
            "display" : "Lymphocyte function antigen-1 defect (disorder)"
          },
          {
            "code" : "23238000",
            "display" : "Common variable agammaglobulinemia (disorder)"
          },
          {
            "code" : "234532001",
            "display" : "Immunodeficiency disorder (disorder)"
          },
          {
            "code" : "234562007",
            "display" : "Anti-protein antibody deficiency (disorder)"
          },
          {
            "code" : "234593008",
            "display" : "Classical complement pathway abnormality (disorder)"
          },
          {
            "code" : "234594002",
            "display" : "Complement 1q deficiency (disorder)"
          },
          {
            "code" : "234595001",
            "display" : "Complement 1q beta chain deficiency (disorder)"
          },
          {
            "code" : "234596000",
            "display" : "Complement 1q dysfunction (disorder)"
          },
          {
            "code" : "234597009",
            "display" : "Complement 1r deficiency (disorder)"
          },
          {
            "code" : "234598004",
            "display" : "Complement 1s deficiency (disorder)"
          },
          {
            "code" : "234599007",
            "display" : "Complement 2 deficiency (disorder)"
          },
          {
            "code" : "234600005",
            "display" : "Complement 4 deficiency (disorder)"
          },
          {
            "code" : "234601009",
            "display" : "Complement 4A deficiency (disorder)"
          },
          {
            "code" : "234602002",
            "display" : "Complement 4B deficiency (disorder)"
          },
          {
            "code" : "234604001",
            "display" : "Alternative pathway deficiency (disorder)"
          },
          {
            "code" : "234605000",
            "display" : "Factor B deficiency (disorder)"
          },
          {
            "code" : "234607008",
            "display" : "Factor D deficiency (disorder)"
          },
          {
            "code" : "234608003",
            "display" : "Terminal component deficiency (disorder)"
          },
          {
            "code" : "234609006",
            "display" : "Complement 5 deficiency (disorder)"
          },
          {
            "code" : "234611002",
            "display" : "Complement 6 deficiency (disorder)"
          },
          {
            "code" : "234612009",
            "display" : "Complement 7 deficiency (disorder)"
          },
          {
            "code" : "234613004",
            "display" : "Combined complement 6 and 7 deficiencies (disorder)"
          },
          {
            "code" : "234614005",
            "display" : "Complement 8 beta chain deficiency (disorder)"
          },
          {
            "code" : "234615006",
            "display" : "Complement 8 beta chain dysfunction (disorder)"
          },
          {
            "code" : "234616007",
            "display" : "Complement 8 alpha-gamma deficiency (disorder)"
          },
          {
            "code" : "234617003",
            "display" : "Complement 9 deficiency (disorder)"
          },
          {
            "code" : "234618008",
            "display" : "Complement regulatory factor defect (disorder)"
          },
          {
            "code" : "234619000",
            "display" : "Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)"
          },
          {
            "code" : "234620006",
            "display" : "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)"
          },
          {
            "code" : "234621005",
            "display" : "Factor I deficiency (disorder)"
          },
          {
            "code" : "234622003",
            "display" : "Factor H deficiency (disorder)"
          },
          {
            "code" : "234623008",
            "display" : "Complement 4 binding protein deficiency (disorder)"
          },
          {
            "code" : "234624002",
            "display" : "Decay accelerating factor deficiency (disorder)"
          },
          {
            "code" : "234625001",
            "display" : "Homologous restriction factor deficiency (disorder)"
          },
          {
            "code" : "234626000",
            "display" : "Complement 5a inhibitor deficiency (disorder)"
          },
          {
            "code" : "234627009",
            "display" : "Anaphylotoxin inactivator deficiency (disorder)"
          },
          {
            "code" : "234628004",
            "display" : "Complement receptor deficiency (disorder)"
          },
          {
            "code" : "234629007",
            "display" : "Complement receptor 1 deficiency (disorder)"
          },
          {
            "code" : "234630002",
            "display" : "Complement receptor 3 deficiency (disorder)"
          },
          {
            "code" : "234631003",
            "display" : "Immunodeficiency with major anomalies (disorder)"
          },
          {
            "code" : "234646005",
            "display" : "Graft-versus-host disease (disorder)"
          },
          {
            "code" : "24419001",
            "display" : "Disorder of complement (disorder)"
          },
          {
            "code" : "24743004",
            "display" : "Complement deficiency disease (disorder)"
          },
          {
            "code" : "263661007",
            "display" : "Complement 5 dysfunction (disorder)"
          },
          {
            "code" : "36070007",
            "display" : "Wiskott-Aldrich syndrome (disorder)"
          },
          {
            "code" : "39674000",
            "display" : "Familial C3B inhibitor deficiency syndrome (disorder)"
          },
          {
            "code" : "402355000",
            "display" : "Acute graft-versus-host disease (disorder)"
          },
          {
            "code" : "402356004",
            "display" : "Chronic graft-versus-host disease (disorder)"
          },
          {
            "code" : "402357008",
            "display" : "Lichenoid chronic graft-versus-host disease (disorder)"
          },
          {
            "code" : "402358003",
            "display" : "Sclerodermoid chronic graft-versus-host disease (disorder)"
          },
          {
            "code" : "402360001",
            "display" : "Materno-fetal graft-versus-host disease (disorder)"
          },
          {
            "code" : "403835002",
            "display" : "X-linked hyper-immunoglobulin M syndrome (disorder)"
          },
          {
            "code" : "403836001",
            "display" : "Autosomal recessive hyperimmunoglobulin M syndrome (disorder)"
          },
          {
            "code" : "403837005",
            "display" : "Wiskott-Aldrich autosomal dominant variant syndrome (disorder)"
          },
          {
            "code" : "414029004",
            "display" : "Disorder of immune function (disorder)"
          },
          {
            "code" : "426202004",
            "display" : "Immune reconstitution syndrome (disorder)"
          },
          {
            "code" : "427167008",
            "display" : "Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)"
          },
          {
            "code" : "442459007",
            "display" : "Combined immunodeficiency disease (disorder)"
          },
          {
            "code" : "444547006",
            "display" : "Graft versus host disease of skin (disorder)"
          },
          {
            "code" : "449187006",
            "display" : "Kappa light chain deficiency (disorder)"
          },
          {
            "code" : "55602000",
            "display" : "Nezelof's syndrome (disorder)"
          },
          {
            "code" : "65880007",
            "display" : "X-linked agammaglobulinemia (disorder)"
          },
          {
            "code" : "702444009",
            "display" : "Autoimmune lymphoproliferative syndrome (disorder)"
          },
          {
            "code" : "719156006",
            "display" : "X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)"
          },
          {
            "code" : "720853005",
            "display" : "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)"
          },
          {
            "code" : "722067005",
            "display" : "Severe combined immunodeficiency with hypereosinophilia (disorder)"
          },
          {
            "code" : "724361001",
            "display" : "Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)"
          },
          {
            "code" : "762618008",
            "display" : "Bronchiolitis obliterans syndrome due to and after lung transplantation (disorder)"
          },
          {
            "code" : "763623001",
            "display" : "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)"
          },
          {
            "code" : "765188009",
            "display" : "Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)"
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          {
            "code" : "771078002",
            "display" : "Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder)"
          },
          {
            "code" : "771443008",
            "display" : "Complement component 3 deficiency (disorder)"
          },
          {
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            "display" : "Primary CD59 deficiency (disorder)"
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          {
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            "display" : "Recurrent Neisseria infection due to factor D deficiency (disorder)"
          },
          {
            "code" : "783248004",
            "display" : "Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection (disorder)"
          },
          {
            "code" : "783249007",
            "display" : "Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder)"
          },
          {
            "code" : "783617001",
            "display" : "Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder)"
          },
          {
            "code" : "783621008",
            "display" : "Immunodeficiency with factor I anomaly (disorder)"
          },
          {
            "code" : "789777007",
            "display" : "Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder)"
          },
          {
            "code" : "81166004",
            "display" : "Properdin deficiency disease (disorder)"
          },
          {
            "code" : "82286005",
            "display" : "Hyperimmunoglobulin M syndrome (disorder)"
          },
          {
            "code" : "82966003",
            "display" : "Hereditary angioedema (disorder)"
          },
          {
            "code" : "846606007",
            "display" : "Graft versus host disease of liver (disorder)"
          },
          {
            "code" : "88714009",
            "display" : "Transient hypogammaglobulinemia of infancy (disorder)"
          }
        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:92bbcf78-2f29-43cb-9ff1-e6fb826c82be",
    "timestamp" : "2024-12-10T10:44:28-05:00",
    "total" : 108,
    "contains" : [
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        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
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        "code" : "1162263002",
        "display" : "Complement component 8 deficiency (disorder)"
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      {
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        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1177120001",
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      {
        "system" : "http://snomed.info/sct",
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        "code" : "1197361002",
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      {
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        "version" : "http://snomed.info/sct/731000124108/version/20240901",
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        "display" : "Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "121121000119106",
        "display" : "Acute graft-versus-host reaction following bone marrow transplant (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
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        "display" : "Chronic graft versus host disease after transplantation of bone marrow (disorder)"
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      {
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        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1268379007",
        "display" : "Graft versus host disease of intestine (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1279887007",
        "display" : "Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "128631000119109",
        "display" : "Chronic graft-versus-host disease following kidney transplant (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
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        "display" : "Complement abnormality (disorder)"
      },
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}

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