[
  {
    "phenotype_id": "PH2289",
    "phenotype_version_id": 5348,
    "name": "Codes for conditions raising risk of severe illness from COVID-19 and not included in the clinically vulnerable criteria",
    "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 `C19MISC_COD` refset published by NHSD.\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": "2026-01-26T22:02:12.689160Z",
    "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": "2026-01-26T22:02:18.730026Z",
    "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": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/c19misc_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/c19misc_cod/20210127",
    "concept_information": [
      {
        "concept_id": 5525,
        "concept_version_id": 13010,
        "concept_name": "nhsd-primary-care-domain-refsets/c19misc_cod/20210127",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2289",
        "phenotype_version_id": 5348,
        "phenotype_name": "Codes for conditions raising risk of severe illness from COVID-19 and not included in the clinically vulnerable criteria",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "111292008",
            "description": "Necrotizing sarcoid granulomatosis",
            "attributes": null
          },
          {
            "code": "111501005",
            "description": "Congenital hereditary muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111502003",
            "description": "Fukuyama congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111503008",
            "description": "Merosin deficient congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111504002",
            "description": "Walker-Warburg congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111505001",
            "description": "Muscle-eye-brain disease, congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111508004",
            "description": "Emery-Dreifuss muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111936002",
            "description": "Cerebral sarcoidosis",
            "attributes": null
          },
          {
            "code": "111937006",
            "description": "Sarcoidosis, nodular type",
            "attributes": null
          },
          {
            "code": "11399002",
            "description": "Pulmonary hypertensive arterial disease",
            "attributes": null
          },
          {
            "code": "117051000119103",
            "description": "Chronic total occlusion of coronary artery",
            "attributes": null
          },
          {
            "code": "124122005",
            "description": "Deficiency of 3-hydroxyacyl-CoA dehydrogenase",
            "attributes": null
          },
          {
            "code": "124166007",
            "description": "Deficiency of butyryl-CoA dehydrogenase",
            "attributes": null
          },
          {
            "code": "124621004",
            "description": "Deficiency of enoyl-coenzyme A hydratase",
            "attributes": null
          },
          {
            "code": "128212001",
            "description": "Spinal muscular atrophy, type II",
            "attributes": null
          },
          {
            "code": "128596003",
            "description": "Medium-chain acyl-coenzyme A dehydrogenase deficiency",
            "attributes": null
          },
          {
            "code": "129642004",
            "description": "Chronic idiopathic immunoneutropenia in adults",
            "attributes": null
          },
          {
            "code": "17363001",
            "description": "Splenic sarcoidosis",
            "attributes": null
          },
          {
            "code": "19057007",
            "description": "Status anginosus",
            "attributes": null
          },
          {
            "code": "192673008",
            "description": "Sarcoid meningitis",
            "attributes": null
          },
          {
            "code": "193101001",
            "description": "Multiple cranial nerve palsies in sarcoidosis",
            "attributes": null
          },
          {
            "code": "193195000",
            "description": "Sarcoid neuropathy",
            "attributes": null
          },
          {
            "code": "193251003",
            "description": "Sarcoid myopathy",
            "attributes": null
          },
          {
            "code": "195033009",
            "description": "Sarcoid heart muscle disease",
            "attributes": null
          },
          {
            "code": "19682006",
            "description": "Lupus hepatitis",
            "attributes": null
          },
          {
            "code": "197368002",
            "description": "Hepatic granulomas in sarcoidosis",
            "attributes": null
          },
          {
            "code": "203042003",
            "description": "Myositis in sarcoidosis",
            "attributes": null
          },
          {
            "code": "205615000",
            "description": "Trisomy 21- meiotic nondisjunction",
            "attributes": null
          },
          {
            "code": "205616004",
            "description": "Trisomy 21- mitotic nondisjunction mosaicism",
            "attributes": null
          },
          {
            "code": "20753005",
            "description": "Hypertensive heart disease complicating AND/OR reason for care during pregnancy",
            "attributes": null
          },
          {
            "code": "21764004",
            "description": "Renal carnitine transport defect",
            "attributes": null
          },
          {
            "code": "21787007",
            "description": "Sarcoidosis, Darier-Roussy type",
            "attributes": null
          },
          {
            "code": "22062008",
            "description": "X-linked glutaric aciduria, type 2",
            "attributes": null
          },
          {
            "code": "22886006",
            "description": "Glutaric aciduria, type 2",
            "attributes": null
          },
          {
            "code": "230193008",
            "description": "Neurosarcoidosis",
            "attributes": null
          },
          {
            "code": "230246005",
            "description": "Progressive bulbar palsy of childhood",
            "attributes": null
          },
          {
            "code": "230247001",
            "description": "Distal spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230248006",
            "description": "Scapuloperoneal spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230249003",
            "description": "Facioscapulohumeral spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230250003",
            "description": "Facioscapulohumeral spinal muscular atrophy with sensory loss",
            "attributes": null
          },
          {
            "code": "230251004",
            "description": "Scapulohumeral spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230252006",
            "description": "Oculopharyngeal spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230253001",
            "description": "Bulbospinal neuronopathy",
            "attributes": null
          },
          {
            "code": "230254007",
            "description": "Western Pacific motor neurone disease",
            "attributes": null
          },
          {
            "code": "230255008",
            "description": "Madras-type motor neurone disease",
            "attributes": null
          },
          {
            "code": "230257000",
            "description": "Paraneoplastic motor neurone disease",
            "attributes": null
          },
          {
            "code": "230258005",
            "description": "Amyotrophic lateral sclerosis with dementia",
            "attributes": null
          },
          {
            "code": "230264003",
            "description": "Troyer syndrome",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "231799005",
            "description": "Sarcoid skin of eyelid",
            "attributes": null
          },
          {
            "code": "232368009",
            "description": "Nasal sarcoidosis",
            "attributes": null
          },
          {
            "code": "232458003",
            "description": "Laryngeal sarcoidosis",
            "attributes": null
          },
          {
            "code": "233743002",
            "description": "Mediastinal lymph node sarcoidosis",
            "attributes": null
          },
          {
            "code": "233744008",
            "description": "Hilar lymph node sarcoidosis",
            "attributes": null
          },
          {
            "code": "233817007",
            "description": "Triple vessel disease of the heart",
            "attributes": null
          },
          {
            "code": "233949008",
            "description": "Pulmonary capillary hemangiomatosis",
            "attributes": null
          },
          {
            "code": "234513007",
            "description": "Post-splenectomy leukocytosis",
            "attributes": null
          },
          {
            "code": "234524009",
            "description": "Sarcoid dactylitis",
            "attributes": null
          },
          {
            "code": "234526006",
            "description": "Ocular sarcoidosis",
            "attributes": null
          },
          {
            "code": "234527002",
            "description": "Lacrimal and parotid gland sarcoidosis",
            "attributes": null
          },
          {
            "code": "234528007",
            "description": "Nasopharyngeal sarcoidosis",
            "attributes": null
          },
          {
            "code": "234529004",
            "description": "Acute sarcoid polymyositis",
            "attributes": null
          },
          {
            "code": "234530009",
            "description": "Chronic sarcoid myopathy",
            "attributes": null
          },
          {
            "code": "234531008",
            "description": "Orofacial sarcoid",
            "attributes": null
          },
          {
            "code": "237997005",
            "description": "Very long chain acyl-coenzyme A dehydrogenase deficiency",
            "attributes": null
          },
          {
            "code": "237999008",
            "description": "Mitochondrial trifunctional protein deficiency",
            "attributes": null
          },
          {
            "code": "238001003",
            "description": "Carnitine palmitoyltransferase I deficiency",
            "attributes": null
          },
          {
            "code": "238002005",
            "description": "Carnitine palmitoyltransferase II deficiency",
            "attributes": null
          },
          {
            "code": "238003000",
            "description": "Carnitine acylcarnitine translocase deficiency",
            "attributes": null
          },
          {
            "code": "238674006",
            "description": "Acute skin sarcoidosis",
            "attributes": null
          },
          {
            "code": "238675007",
            "description": "Sarcoidosis-induced erythema nodosum",
            "attributes": null
          },
          {
            "code": "238677004",
            "description": "Maculopapular sarcoidosis",
            "attributes": null
          },
          {
            "code": "238678009",
            "description": "Chronic skin sarcoidosis",
            "attributes": null
          },
          {
            "code": "238679001",
            "description": "Sarcoidosis in scar",
            "attributes": null
          },
          {
            "code": "238680003",
            "description": "Papular sarcoidosis",
            "attributes": null
          },
          {
            "code": "238681004",
            "description": "Lichenoid sarcoidosis",
            "attributes": null
          },
          {
            "code": "240047005",
            "description": "X-linked muscular dystrophy with limb girdle distribution",
            "attributes": null
          },
          {
            "code": "240048000",
            "description": "X-linked muscular dystrophy with abnormal dystrophin",
            "attributes": null
          },
          {
            "code": "240049008",
            "description": "Intermediate X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240050008",
            "description": "Manifesting female carrier of X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240051007",
            "description": "X-linked limb girdle muscular dystrophy with normal dystrophin",
            "attributes": null
          },
          {
            "code": "240052000",
            "description": "Ji muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240053005",
            "description": "Hereditary myopathy limited to females",
            "attributes": null
          },
          {
            "code": "240055003",
            "description": "Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein",
            "attributes": null
          },
          {
            "code": "240058001",
            "description": "Reunion-Indiana Amish type muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240060004",
            "description": "Western type of congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240061000",
            "description": "Congenital muscular dystrophy with arthrogryposis multiplex congenita",
            "attributes": null
          },
          {
            "code": "240062007",
            "description": "Ullrich congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240063002",
            "description": "Eichsfeld type congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240064008",
            "description": "Hutterite type of muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240071003",
            "description": "X-linked muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240072005",
            "description": "Benign scapuloperoneal muscular dystrophy with cardiomyopathy",
            "attributes": null
          },
          {
            "code": "240073000",
            "description": "Autosomal recessive muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240074006",
            "description": "Scapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240075007",
            "description": "Autosomal dominant muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240076008",
            "description": "Benign scapuloperoneal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240078009",
            "description": "Benign congenital muscular dystrophy with finger flexion contractures",
            "attributes": null
          },
          {
            "code": "24829000",
            "description": "Eosinophilic ulcerative colitis",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "253356004",
            "description": "Left atrial appendage absent",
            "attributes": null
          },
          {
            "code": "25425008",
            "description": "Autosomal recessive glutaric aciduria, type 2",
            "attributes": null
          },
          {
            "code": "254264002",
            "description": "Partial trisomy 21 in Down's syndrome",
            "attributes": null
          },
          {
            "code": "26950008",
            "description": "Chronic ectopic atrial tachycardia",
            "attributes": null
          },
          {
            "code": "276517000",
            "description": "Transient myocardial ischemia of newborn",
            "attributes": null
          },
          {
            "code": "276518005",
            "description": "Transient tricuspid regurgitation of newborn",
            "attributes": null
          },
          {
            "code": "278928000",
            "description": "Transient mitral regurgitation of newborn",
            "attributes": null
          },
          {
            "code": "281091000",
            "description": "Ischemic myocardial dysfunction",
            "attributes": null
          },
          {
            "code": "281093002",
            "description": "Hibernating myocardium",
            "attributes": null
          },
          {
            "code": "282006",
            "description": "Acute myocardial infarction of basal-lateral wall",
            "attributes": null
          },
          {
            "code": "28248000",
            "description": "Left anterior descending coronary artery thrombosis",
            "attributes": null
          },
          {
            "code": "286947004",
            "description": "Chronic rheumatic mitral valve",
            "attributes": null
          },
          {
            "code": "286950001",
            "description": "Chronic rheumatic aortic valve disease",
            "attributes": null
          },
          {
            "code": "305719002",
            "description": "Neuromyotonia",
            "attributes": null
          },
          {
            "code": "307127004",
            "description": "Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency",
            "attributes": null
          },
          {
            "code": "307128009",
            "description": "Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency",
            "attributes": null
          },
          {
            "code": "307130006",
            "description": "3-Ketoacyl-coenzyme A triolase deficiency",
            "attributes": null
          },
          {
            "code": "310607007",
            "description": "Sarcoidosis of inferior turbinates",
            "attributes": null
          },
          {
            "code": "31097004",
            "description": "Post poliomyelitis syndrome",
            "attributes": null
          },
          {
            "code": "312930008",
            "description": "Sarcoid chorioretinitis",
            "attributes": null
          },
          {
            "code": "31541009",
            "description": "Sarcoidosis",
            "attributes": null
          },
          {
            "code": "352941000119102",
            "description": "Sarcoid iridocyclitis",
            "attributes": null
          },
          {
            "code": "361197009",
            "description": "Sarcoid arthropathy",
            "attributes": null
          },
          {
            "code": "361198004",
            "description": "Sarcoid arthritis",
            "attributes": null
          },
          {
            "code": "37061001",
            "description": "Granulomatous sarcoid nephropathy",
            "attributes": null
          },
          {
            "code": "37340000",
            "description": "Motor neuron disease",
            "attributes": null
          },
          {
            "code": "387732009",
            "description": "Becker muscular dystrophy",
            "attributes": null
          },
          {
            "code": "39041004",
            "description": "Restrictive cardiomyopathy secondary to sarcoidosis",
            "attributes": null
          },
          {
            "code": "398432008",
            "description": "Bulbar weakness",
            "attributes": null
          },
          {
            "code": "399091004",
            "description": "Facioscapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "400127001",
            "description": "Sarcoidal granuloma of skin",
            "attributes": null
          },
          {
            "code": "402368008",
            "description": "Ichthyosiform sarcoidosis",
            "attributes": null
          },
          {
            "code": "402369000",
            "description": "Atrophic sarcoidosis",
            "attributes": null
          },
          {
            "code": "402370004",
            "description": "Ulcerative sarcoidosis",
            "attributes": null
          },
          {
            "code": "402371000",
            "description": "Verrucous sarcoidosis",
            "attributes": null
          },
          {
            "code": "402372007",
            "description": "Subcutaneous nodular sarcoidosis",
            "attributes": null
          },
          {
            "code": "402373002",
            "description": "Hypomelanotic sarcoidosis",
            "attributes": null
          },
          {
            "code": "402374008",
            "description": "Nail dystrophy due to sarcoidosis",
            "attributes": null
          },
          {
            "code": "402379003",
            "description": "Talc granuloma of umbilicus",
            "attributes": null
          },
          {
            "code": "408335007",
            "description": "Autoimmune hepatitis",
            "attributes": null
          },
          {
            "code": "41040004",
            "description": "Complete trisomy 21 syndrome",
            "attributes": null
          },
          {
            "code": "415359008",
            "description": "Sarcoid uveitis",
            "attributes": null
          },
          {
            "code": "421671002",
            "description": "Pneumonia associated with acquired immunodeficiency syndrome",
            "attributes": null
          },
          {
            "code": "425384007",
            "description": "Sarcoidosis with glomerulonephritis",
            "attributes": null
          },
          {
            "code": "4416007",
            "description": "Heerfordt's syndrome",
            "attributes": null
          },
          {
            "code": "44395000",
            "description": "Spastic tetraplegia with rigidity syndrome",
            "attributes": null
          },
          {
            "code": "46251005",
            "description": "Corticospinal motor disease",
            "attributes": null
          },
          {
            "code": "472757001",
            "description": "Pulmonary venous hypertension as complication of procedure",
            "attributes": null
          },
          {
            "code": "472758006",
            "description": "Pulmonary venous hypertension due to compression of pulmonary great vein",
            "attributes": null
          },
          {
            "code": "472759003",
            "description": "Pulmonary venous hypertension due to compression of pulmonary great vein by sclerosing mediastinitis",
            "attributes": null
          },
          {
            "code": "472760008",
            "description": "Pulmonary venous hypertension due to compression of pulmonary great vein by lymphadenopathy",
            "attributes": null
          },
          {
            "code": "472761007",
            "description": "Pulmonary venous hypertension due to compression of pulmonary great vein by neoplasm",
            "attributes": null
          },
          {
            "code": "472785004",
            "description": "Right ventricular outflow tract obstruction due to neoplasm",
            "attributes": null
          },
          {
            "code": "472786003",
            "description": "Right ventricular outflow tract obstruction due to foreign body",
            "attributes": null
          },
          {
            "code": "472787007",
            "description": "Left ventricular outflow tract obstruction due to neoplasm",
            "attributes": null
          },
          {
            "code": "472790001",
            "description": "Pulmonary venous hypertension due to disorder of left heart",
            "attributes": null
          },
          {
            "code": "472803004",
            "description": "Acquired abnormality of atrioventricular (not morphologically mitral or tricuspid) valve associated with atrioventricular septal defect",
            "attributes": null
          },
          {
            "code": "49793008",
            "description": "Hereditary motor neuron disease",
            "attributes": null
          },
          {
            "code": "5262007",
            "description": "Spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "54280009",
            "description": "Kugelberg-Welander disease",
            "attributes": null
          },
          {
            "code": "54304004",
            "description": "Progressive bulbar palsy",
            "attributes": null
          },
          {
            "code": "54515008",
            "description": "Sarcoidosis, plaque type",
            "attributes": null
          },
          {
            "code": "5499009",
            "description": "Pulmonary hypertensive venous disease",
            "attributes": null
          },
          {
            "code": "55016009",
            "description": "Congenital muscular hypertrophy-cerebral syndrome",
            "attributes": null
          },
          {
            "code": "55941000",
            "description": "Cutaneous sarcoidosis",
            "attributes": null
          },
          {
            "code": "58870009",
            "description": "Sarcoidosis, anular type",
            "attributes": null
          },
          {
            "code": "6022005",
            "description": "Dilated cardiomyopathy secondary to sarcoidosis",
            "attributes": null
          },
          {
            "code": "62350000",
            "description": "Starch granuloma of skin",
            "attributes": null
          },
          {
            "code": "64383006",
            "description": "Werdnig-Hoffmann disease",
            "attributes": null
          },
          {
            "code": "6471000179103",
            "description": "Transplantation of kidney and pancreas",
            "attributes": null
          },
          {
            "code": "64757003",
            "description": "Lymph node sarcoidosis",
            "attributes": null
          },
          {
            "code": "6661000119101",
            "description": "Coronary arteriosclerosis in native artery of transplanted heart",
            "attributes": null
          },
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