[
  {
    "phenotype_id": "PH2616",
    "phenotype_version_id": 6453,
    "name": "Codes required for COVID-19 pandemic planning and research not included within associated clusters from other services to be returned with no time limit",
    "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nTaken from the `GDPPRMISC_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3\\.0 (https://www.nationalarchives.gov.uk/doc/open\\-government\\-licence/version/3/).\n\n\n© University of Oxford for the Bennett Institute for Applied Data Science 2025\\. This work may be copied freely for non\\-commercial research and study.\n\n",
    "implementation": null,
    "publications": null,
    "validation": null,
    "citation_requirements": null,
    "created": "2026-01-26T22:29:07.556127Z",
    "author": "NHSD Primary Care Domain Refsets",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T22:29:12.060610Z",
    "references": [
      {
        "url": "https://digital.nhs.uk/data-and-information/data-collections-and-data-sets/data-collections/quality-and-outcomes-framework-qof/quality-and-outcome-framework-qof-business-rules/primary-care-domain-reference-set-portal",
        "title": "Primary Care Domain Reference Set Portal"
      }
    ],
    "signed_off": [],
    "methodology": "This codelist was imported automatically. The following codes were not found in the SNOMED CT (UK Clinical Edition) dictionary and so excluded from this codelist: 16649411000001104, 40085311000001103, 40085011000001101, 34680411000001107, 16649511000001100, 39566211000001103, 35727111000001109\\.\n\n\nThis may be because this codelist contains both clinical terms and medications. In which case you may need to create another codelist for the missing clinical/medication codes.\n\n",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/gdpprmisc_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/gdpprmisc_cod/20250912",
    "concept_information": [
      {
        "concept_id": 6630,
        "concept_version_id": 14115,
        "concept_name": "nhsd-primary-care-domain-refsets/gdpprmisc_cod/20250912",
        "coding_system": {
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          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2616",
        "phenotype_version_id": 6453,
        "phenotype_name": "Codes required for COVID-19 pandemic planning and research not included within associated clusters from other services to be returned with no time limit",
        "code_attribute_header": [],
        "codes": [
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            "description": "Lesch-Nyhan syndrome",
            "attributes": null
          },
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            "description": "Capsular tear without major disruption of parenchyma of spleen AND with open wound in abdominal cavity",
            "attributes": null
          },
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            "code": "1156774008",
            "description": "Rheumatoid factor positive and cyclic citrullinated peptide antibody positive juvenile polyarthritis",
            "attributes": null
          },
          {
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            "description": "Rheumatoid factor positive and cyclic citrullinated peptide antibody negative juvenile polyarthritis",
            "attributes": null
          },
          {
            "code": "1162462009",
            "description": "Angelman syndrome due to maternal monosomy 15q11q13",
            "attributes": null
          },
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            "code": "1172696009",
            "description": "Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome",
            "attributes": null
          },
          {
            "code": "1172899000",
            "description": "Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome",
            "attributes": null
          },
          {
            "code": "1173024006",
            "description": "Typical absence seizure",
            "attributes": null
          },
          {
            "code": "1186711002",
            "description": "G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome",
            "attributes": null
          },
          {
            "code": "1186863001",
            "description": "Arginine vasopressin deficiency due to trauma",
            "attributes": null
          },
          {
            "code": "1187045009",
            "description": "Aicardi Goutieres syndrome type 1",
            "attributes": null
          },
          {
            "code": "1187046005",
            "description": "Aicardi Goutieres syndrome type 2",
            "attributes": null
          },
          {
            "code": "1187047001",
            "description": "Aicardi Goutieres syndrome type 3",
            "attributes": null
          },
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            "code": "1187048006",
            "description": "Aicardi Goutieres syndrome type 4",
            "attributes": null
          },
          {
            "code": "1187049003",
            "description": "Aicardi Goutieres syndrome type 5",
            "attributes": null
          },
          {
            "code": "1208966001",
            "description": "Generalized onset motor epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208968000",
            "description": "Generalized onset atonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208969008",
            "description": "Generalized onset tonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208970009",
            "description": "Generalized onset clonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208971008",
            "description": "Generalized onset myoclonic-atonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208972001",
            "description": "Generalized onset myoclonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208973006",
            "description": "Generalized onset myoclonic-tonic-clonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1208991001",
            "description": "Myoclonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1217209006",
            "description": "Generalized onset tonic-clonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "1236975007",
            "description": "Behavioral arrest epileptic seizure",
            "attributes": null
          },
          {
            "code": "1239381000000101",
            "description": "Haemoglobin E beta plus thalassaemia",
            "attributes": null
          },
          {
            "code": "1263997005",
            "description": "Metastatic pilomatrix carcinoma to skin",
            "attributes": null
          },
          {
            "code": "127067009",
            "description": "Stress neutrophilia",
            "attributes": null
          },
          {
            "code": "129639005",
            "description": "Hereditary neutrophilia",
            "attributes": null
          },
          {
            "code": "133841000119105",
            "description": "Merkel cell carcinoma of face",
            "attributes": null
          },
          {
            "code": "15182000",
            "description": "Coffin-Lowry syndrome",
            "attributes": null
          },
          {
            "code": "15285008",
            "description": "Adenylosuccinate lyase deficiency",
            "attributes": null
          },
          {
            "code": "16058671000119103",
            "description": "Transplant rejection of cornea of left eye",
            "attributes": null
          },
          {
            "code": "16058711000119104",
            "description": "Transplant failure of cornea of right eye",
            "attributes": null
          },
          {
            "code": "16058831000119102",
            "description": "Transplant rejection of cornea of right eye",
            "attributes": null
          },
          {
            "code": "16058871000119104",
            "description": "Transplant failure of cornea of left eye",
            "attributes": null
          },
          {
            "code": "16196000",
            "description": "Infectious mononucleosis caused by Cytomegalovirus",
            "attributes": null
          },
          {
            "code": "16294009",
            "description": "Splenomegaly",
            "attributes": null
          },
          {
            "code": "165531008",
            "description": "Lymphocytosis - absolute",
            "attributes": null
          },
          {
            "code": "16873003",
            "description": "Musicogenic seizure",
            "attributes": null
          },
          {
            "code": "16944002",
            "description": "Mononucleosis syndrome",
            "attributes": null
          },
          {
            "code": "17122004",
            "description": "4p partial monosomy syndrome",
            "attributes": null
          },
          {
            "code": "184293009",
            "description": "Patient died at home",
            "attributes": null
          },
          {
            "code": "184295002",
            "description": "Patient died in nursing home",
            "attributes": null
          },
          {
            "code": "184298000",
            "description": "Patient died in street",
            "attributes": null
          },
          {
            "code": "19058002",
            "description": "Congestive splenomegaly",
            "attributes": null
          },
          {
            "code": "191273000",
            "description": "Leukemoid reaction of the newborn",
            "attributes": null
          },
          {
            "code": "191667009",
            "description": "Paranoid disorder",
            "attributes": null
          },
          {
            "code": "192981006",
            "description": "Atonic epileptic seizure",
            "attributes": null
          },
          {
            "code": "192982004",
            "description": "Epileptic seizures - akinetic",
            "attributes": null
          },
          {
            "code": "192991000",
            "description": "Clonic epileptic seizure",
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          },
          {
            "code": "192993002",
            "description": "Tonic epileptic seizure",
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          },
          {
            "code": "19636003",
            "description": "Monocytosis",
            "attributes": null
          },
          {
            "code": "205788004",
            "description": "Fetal alcohol syndrome",
            "attributes": null
          },
          {
            "code": "230273006",
            "description": "Frontotemporal degeneration",
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          },
          {
            "code": "230447004",
            "description": "Absence seizure with eyelid myoclonia",
            "attributes": null
          },
          {
            "code": "230458008",
            "description": "Atypical absence status epilepticus",
            "attributes": null
          },
          {
            "code": "234434003",
            "description": "Alders syndrome",
            "attributes": null
          },
          {
            "code": "234620006",
            "description": "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor",
            "attributes": null
          },
          {
            "code": "23833000",
            "description": "Poisoning caused by antineoplastic AND/OR immunosuppressive drug",
            "attributes": null
          },
          {
            "code": "238975005",
            "description": "Delusion of foul odor",
            "attributes": null
          },
          {
            "code": "239910001",
            "description": "Toxic oil syndrome",
            "attributes": null
          },
          {
            "code": "240789006",
            "description": "Hepatosplenic schistosomiasis",
            "attributes": null
          },
          {
            "code": "240790002",
            "description": "Schistosomal hepatomegaly",
            "attributes": null
          },
          {
            "code": "240791003",
            "description": "Hepatic schistosomal granuloma",
            "attributes": null
          },
          {
            "code": "240792005",
            "description": "Symmer's pipe-stem fibrosis",
            "attributes": null
          },
          {
            "code": "240793000",
            "description": "Schistosomal splenomegaly",
            "attributes": null
          },
          {
            "code": "246551007",
            "description": "Absence seizure with automatisms",
            "attributes": null
          },
          {
            "code": "2593002",
            "description": "Dubowitz's syndrome",
            "attributes": null
          },
          {
            "code": "267454002",
            "description": "Acatalasemia",
            "attributes": null
          },
          {
            "code": "278484009",
            "description": "Tropical pulmonary eosinophilia",
            "attributes": null
          },
          {
            "code": "278855005",
            "description": "Frontal lobe degeneration",
            "attributes": null
          },
          {
            "code": "29789008",
            "description": "Monocytic leukemoid reaction",
            "attributes": null
          },
          {
            "code": "2990008",
            "description": "Lymphocytic leukemoid reaction",
            "attributes": null
          },
          {
            "code": "302823005",
            "description": "Glucagonoma",
            "attributes": null
          },
          {
            "code": "302835009",
            "description": "Pheochromocytoma",
            "attributes": null
          },
          {
            "code": "304215001",
            "description": "Patient died during operation",
            "attributes": null
          },
          {
            "code": "313307000",
            "description": "Epileptic seizure",
            "attributes": null
          },
          {
            "code": "313372007",
            "description": "Patient died in hospice",
            "attributes": null
          },
          {
            "code": "33301000119105",
            "description": "Sequela of cardioembolic stroke",
            "attributes": null
          },
          {
            "code": "33982008",
            "description": "Hyperphosphatasemia with intellectual disability",
            "attributes": null
          },
          {
            "code": "37180002",
            "description": "Chronic nonspecific lung disease",
            "attributes": null
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          {
            "code": "394702007",
            "description": "Chronic obstructive pulmonary disease follow-up",
            "attributes": null
          },
          {
            "code": "394703002",
            "description": "Chronic obstructive pulmonary disease annual review",
            "attributes": null
          },
          {
            "code": "397007003",
            "description": "Mast cell disorder",
            "attributes": null
          },
          {
            "code": "403767009",
            "description": "Acrocephalopolysyndactyly type II",
            "attributes": null
          },
          {
            "code": "40425004",
            "description": "Postconcussion syndrome",
            "attributes": null
          },
          {
            "code": "410796000",
            "description": "Juvenile seropositive polyarthritis",
            "attributes": null
          },
          {
            "code": "413150001",
            "description": "Patient died in general practice premises",
            "attributes": null
          },
          {
            "code": "41466009",
            "description": "Myocardial imaging for infarct with ejection fraction, first pass technique",
            "attributes": null
          },
          {
            "code": "420300004",
            "description": "New York Heart Association Classification - Class I",
            "attributes": null
          },
          {
            "code": "420913000",
            "description": "New York Heart Association Classification - Class III",
            "attributes": null
          },
          {
            "code": "421460008",
            "description": "Retinopathy with acquired immunodeficiency syndrome",
            "attributes": null
          },
          {
            "code": "421704003",
            "description": "New York Heart Association Classification - Class II",
            "attributes": null
          },
          {
            "code": "422293003",
            "description": "New York Heart Association Classification - Class IV",
            "attributes": null
          },
          {
            "code": "422348008",
            "description": "Andersen Tawil syndrome",
            "attributes": null
          },
          {
            "code": "432636005",
            "description": "Administration of vaccine product containing only Human alphaherpesvirus 3 and Measles morbillivirus and Mumps orthorubulavirus and Rubella virus antigens",
            "attributes": null
          },
          {
            "code": "433733003",
            "description": "Administration of second dose of vaccine product containing only Human alphaherpesvirus 3 and Measles morbillivirus and Mumps orthorubulavirus and Rubella virus antigens",
            "attributes": null
          },
          {
            "code": "449817000",
            "description": "Peters plus syndrome",
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          },
          {
            "code": "45864009",
            "description": "Senile degeneration of brain",
            "attributes": null
          },
          {
            "code": "46288008",
            "description": "Payr's syndrome",
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          {
            "code": "47986005",
            "description": "Genetic anomaly of leukocyte",
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          },
          {
            "code": "502521000000103",
            "description": "[D]Death, not violent/instantaneous",
            "attributes": null
          },
          {
            "code": "508171000000105",
            "description": "Severe learning disability",
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          },
          {
            "code": "54898003",
            "description": "Multiple sulfatase deficiency",
            "attributes": null
          },
          {
            "code": "5619004",
            "description": "Bardet-Biedl syndrome",
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          },
          {
            "code": "56478004",
            "description": "Leukemoid reaction",
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          },
          {
            "code": "572511000119105",
            "description": "Administration of vaccine product containing only live attenuated Measles morbillivirus and Mumps orthorubulavirus and Rubella virus and Human alphaherpesvirus 3 antigens",
            "attributes": null
          },
          {
            "code": "59399004",
            "description": "Cutis laxa, x-linked",
            "attributes": null
          },
          {
            "code": "613003",
            "description": "Fragile X syndrome",
            "attributes": null
          },
          {
            "code": "61596005",
            "description": "Heterophil-positive mononucleosis syndrome",
            "attributes": null
          },
          {
            "code": "63119004",
            "description": "Weaver syndrome",
            "attributes": null
          },
          {
            "code": "63670007",
            "description": "Myocardial imaging for infarct, planar technique",
            "attributes": null
          },
          {
            "code": "64936001",
            "description": "Löffler's syndrome",
            "attributes": null
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          {
            "code": "65230006",
            "description": "Heterophil-negative mononucleosis syndrome",
            "attributes": null
          },
          {
            "code": "67023009",
            "description": "Lymphocytosis",
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          {
            "code": "67155006",
            "description": "Gerstmann-Straussler-Scheinker syndrome",
            "attributes": null
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          {
            "code": "685101000119106",
            "description": "Hemoglobin E beta plus thalassemia",
            "attributes": null
          },
          {
            "code": "698747008",
            "description": "Patient died in care home",
            "attributes": null
          },
          {
            "code": "699297004",
            "description": "Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type",
            "attributes": null
          },
          {
            "code": "700215003",
            "description": "Patient died in usual place of residence",
            "attributes": null
          },
          {
            "code": "7033004",
            "description": "Absence status epilepticus",
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          },
          {
            "code": "70349007",
            "description": "Pseudoneutrophilia",
            "attributes": null
          },
          {
            "code": "703535000",
            "description": "Mowat-Wilson syndrome",
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          },
          {
            "code": "710926008",
            "description": "Periodontitis co-occurrent with familial neutropenia",
            "attributes": null
          },
          {
            "code": "713742005",
            "description": "Human immunodeficiency virus antibody detected",
            "attributes": null
          },
          {
            "code": "71610005",
            "description": "Neutrophilic leukemoid reaction",
            "attributes": null
          },
          {
            "code": "716709002",
            "description": "FRAXE intellectual disability syndrome",
            "attributes": null
          },
          {
            "code": "71692003",
            "description": "Leukoerythroblastotic reaction",
            "attributes": null
          },
          {
            "code": "717223008",
            "description": "X-linked epilepsy with learning disability and behavior disorder syndrome",
            "attributes": null
          },
          {
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            "description": "Spondyloepiphyseal dysplasia tarda Kohn type",
            "attributes": null
          },
          {
            "code": "719842006",
            "description": "Congenital hypoplasia of ulna and intellectual disability syndrome",
            "attributes": null
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            "description": "Arachnodactyly with abnormal ossification and intellectual disability syndrome",
            "attributes": null
          },
          {
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            "description": "Contracture with ectodermal dysplasia and orofacial cleft syndrome",
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          {
            "code": "721974000",
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          {
            "code": "723365002",
            "description": "Hypotrichosis and intellectual disability syndrome Lopes type",
            "attributes": null
          },
          {
            "code": "723504000",
            "description": "Ramos Arroyo syndrome",
            "attributes": null
          },
          {
            "code": "723621000",
            "description": "Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome",
            "attributes": null
          },
          {
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            "description": "Macrocephaly, obesity, mental disability, ocular abnormality syndrome",
            "attributes": null
          },
          {
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            "description": "Splenomegaly co-occurrent and due to storage disease",
            "attributes": null
          },
          {
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            "description": "Bullous dystrophy macular type",
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          {
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            "description": "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome",
            "attributes": null
          },
          {
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            "description": "Preaxial polydactyly, colobomata, intellectual disability syndrome",
            "attributes": null
          },
          {
            "code": "733472005",
            "description": "Microcephalus, glomerulonephritis, marfanoid habitus syndrome",
            "attributes": null
          },
          {
            "code": "737081007",
            "description": "Administration of vaccine product containing only Human alphaherpesvirus 3 antigen for chickenpox",
            "attributes": null
          },
          {
            "code": "74263009",
            "description": "Carpenter syndrome",
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          },
          {
            "code": "74509007",
            "description": "Death by cremation",
            "attributes": null
          },
          {
            "code": "7573000",
            "description": "Classical phenylketonuria",
            "attributes": null
          },
          {
            "code": "763618001",
            "description": "Wiedemann Steiner syndrome",
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          {
            "code": "763795006",
            "description": "Malan overgrowth syndrome",
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          {
            "code": "763837007",
            "description": "Oro-facial digital syndrome type 14",
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          },
          {
            "code": "7689009",
            "description": "Reading seizure",
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          },
          {
            "code": "771471002",
            "description": "Optic nerve edema, splenomegaly syndrome",
            "attributes": null
          },
          {
            "code": "773622005",
            "description": "Craniofacial dysplasia osteopenia syndrome",
            "attributes": null
          },
          {
            "code": "77527000",
            "description": "9p partial trisomy syndrome",
            "attributes": null
          },
          {
            "code": "783006001",
            "description": "Low-grade neuroendocrine neoplasm of corpus uteri",
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          },
          {
            "code": "783089006",
            "description": "Macrocephaly, intellectual disability, autism syndrome",
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          {
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            "description": "Armanni-Ebstein kidney due to diabetes mellitus",
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          },
          {
            "code": "79631006",
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          },
          {
            "code": "80369006",
            "description": "Chronic neutrophilia",
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          },
          {
            "code": "80378000",
            "description": "Neonatal hepatosplenomegaly",
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          },
          {
            "code": "83157008",
            "description": "Fatal familial insomnia",
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          },
          {
            "code": "85559002",
            "description": "Pelger-Huët anomaly",
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          },
          {
            "code": "86188000",
            "description": "Kuru",
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          },
          {
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