COVID19 metabolic underlying condition reference set

{
  "compose" : {
    "exclude" : [ ],
    "include" : [ {
      "system" : "http://snomed.info/sct",
      "extension" : [ {
        "extension" : [ {
          "valueString" : "concept",
          "url" : "path"
        }, {
          "url" : "count",
          "valueInteger" : 96
        } ],
        "url" : "http://health-samurai.io/extensions/excised-data"
      } ]
    } ]
  },
  "date" : "2020-09-03T01:00:25-04:00",
  "meta" : {
    "versionId" : "14",
    "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" ]
  },
  "publisher" : "HSPC Steward",
  "jurisdiction" : [ {
    "coding" : [ {
      "system" : "urn:iso:std:iso:3166",
      "code" : "US"
    } ]
  } ],
  "purpose" : "(Clinical Focus: COVID19 metabolic underlying condition value set as defined by the Clinical Information Modeling Initiative.),(Data Element Scope: The purpose of this reference set is to document underlying metabolic conditions described in COVID-19 case reporting forms, resulting the SNOMED CT concept: COVID-19 metabolic underlying condition reference set (foundation metadata concept) [25571000205100]),(Inclusion Criteria: ),(Exclusion Criteria: )",
  "name" : "COVID19MetabolicUnderlyingConditionReferenceSet",
  "experimental" : false,
  "resourceType" : "ValueSet",
  "expansion" : {
    "contains" : [ {
      "system" : "http://snomed.info/sct",
      "code" : "10649000",
      "display" : "Hyperpituitarism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "111385000",
      "display" : "Tay-Sachs disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "11179002",
      "display" : "Glycogen storage disease, type IV (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "124302001",
      "display" : "Deficiency of galactokinase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "124329006",
      "display" : "Deficiency of phosphorylase kinase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "124335006",
      "display" : "Deficiency of phosphoglycerate kinase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "124437004",
      "display" : "Deficiency of glucose-6-phosphatase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "124675005",
      "display" : "Deficiency of phosphoglycerate mutase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "128289001",
      "display" : "Chronic metabolic disorder (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "16652001",
      "display" : "Fabry's disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "18756002",
      "display" : "Juvenile GM1 gangliosidosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "190680002",
      "display" : "Disorders of amino acid transport and metabolism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "190745006",
      "display" : "Galactosemia (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "190794006",
      "display" : "Glucosylceramide beta-glucosidase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "192782005",
      "display" : "Galactosylceramide beta-galactosidase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "20052008",
      "display" : "Fructose-1,6-bisphosphate aldolase B deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "21983002",
      "display" : "Hashimoto thyroiditis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "235908005",
      "display" : "Glycogen storage disease type IX (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "237602007",
      "display" : "Metabolic syndrome X (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "237735008",
      "display" : "Adrenal Cushing's syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "237751000",
      "display" : "Congenital adrenal hyperplasia (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "237964009",
      "display" : "Glycogen synthase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238006008",
      "display" : "Disorder of purine and pyrimidine metabolism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238025006",
      "display" : "GM1 gangliosidosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238059005",
      "display" : "Disorder of peroxisomal function (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238061001",
      "display" : "Neonatal adrenoleukodystrophy (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238062008",
      "display" : "Infantile Refsum's disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238068007",
      "display" : "Bifunctional peroxisomal enzyme deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "238069004",
      "display" : "Acyl-coenzyme A oxidase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "23849003",
      "display" : "Sandhoff disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "25362006",
      "display" : "Phytanic acid storage disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "264580006",
      "display" : "Thyroid dysfunction (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "26745009",
      "display" : "Mucopolysaccharidosis type I-H/S (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "267454002",
      "display" : "Acatalasemia (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "274864009",
      "display" : "Glycogen storage disease, type II (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "27718001",
      "display" : "Maple syrup urine disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "28183005",
      "display" : "Fructose-biphosphatase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "29291001",
      "display" : "Glycogen storage disease, type VI (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "30171000",
      "display" : "Disorder of adrenal gland (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "34420000",
      "display" : "Storage disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "34486009",
      "display" : "Hyperthyroidism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "353295004",
      "display" : "Graves' disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "35691006",
      "display" : "Combined deficiency of sialidase AND beta galactosidase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "363732003",
      "display" : "Addison's disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "367368009",
      "display" : "Sulfite oxidase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "36976004",
      "display" : "Hypoparathyroidism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "37666005",
      "display" : "Glycogen storage disease type X (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "378007",
      "display" : "Morquio syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "386584007",
      "display" : "Adrenal cortical hypofunction (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "387817006",
      "display" : "Deficiency of phosphorylase b kinase (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "38795005",
      "display" : "Sialidosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "396338004",
      "display" : "Metachromatic leucodystrophy (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "399244003",
      "display" : "Disorder of pituitary gland (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "40930008",
      "display" : "Hypothyroidism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "41527003",
      "display" : "Glycogen storage disease type VIII (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "419097006",
      "display" : "Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "43916004",
      "display" : "Mucopolysaccharidosis type VII (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "44054006",
      "display" : "Diabetes mellitus type 2 (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "45744005",
      "display" : "Disorder of mineral metabolism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "46635009",
      "display" : "Diabetes mellitus type 1 (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "46683007",
      "display" : "Pyruvate dehydrogenase complex deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "5335002",
      "display" : "Phosphoenolpyruvate carboxykinase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "54954004",
      "display" : "Aspartylglucosaminuria (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "55912009",
      "display" : "Glycogen storage disease, type V (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "58459009",
      "display" : "Sphingomyelin/cholesterol lipidosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "61598006",
      "display" : "Glycogenosis with glucoaminophosphaturia (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "65327002",
      "display" : "Mucopolysaccharidosis type I-H (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "65389002",
      "display" : "Adrenoleukodystrophy (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "65520001",
      "display" : "Primary hyperoxaluria, type I (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "65524005",
      "display" : "Mannosidosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "65764006",
      "display" : "Pseudo-Hurler polydystrophy (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "66937008",
      "display" : "Glycogen storage disease, type III (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "66999008",
      "display" : "Hyperparathyroidism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "69463008",
      "display" : "Maroteaux-Lamy syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "700463002",
      "display" : "Alpha-methylacyl-CoA racemase deficiency disorder (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "70199000",
      "display" : "I-cell disease (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "70737009",
      "display" : "Mucopolysaccharidosis type II (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "717276003",
      "display" : "Folinic acid responsive seizure syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "717821004",
      "display" : "Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "725296006",
      "display" : "Mucolipidosis type IV (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "7265005",
      "display" : "Glycogen storage disease, type I (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "73123008",
      "display" : "Mucopolysaccharidosis type I-S (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "73132005",
      "display" : "Disorder of parathyroid gland (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "73211009",
      "display" : "Diabetes mellitus (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "734434007",
      "display" : "Pyridoxine-dependent epilepsy (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "74728003",
      "display" : "Hypopituitarism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "75610003",
      "display" : "Mucopolysaccharidosis type I (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "7573000",
      "display" : "Classical phenylketonuria (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "783717008",
      "display" : "Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "79935000",
      "display" : "Farber's lipogranulomatosis (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "86095007",
      "display" : "Inborn error of metabolism (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "88393000",
      "display" : "Sanfilippo syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "88469006",
      "display" : "Zellweger syndrome (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "8849004",
      "display" : "Uridine diphosphate glucose-4-epimerase deficiency (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    }, {
      "system" : "http://snomed.info/sct",
      "code" : "89597008",
      "display" : "Glycogen storage disease, type VII (disorder)",
      "version" : "http://snomed.info/sct/731000124108/version/20230901"
    } ],
    "total" : 95,
    "identifier" : "urn:uuid:9f118bfd-445b-4539-ab02-46135cf9deb0",
    "timestamp" : "2024-04-23T10:17:02-04:00"
  },
  "title" : "COVID19 metabolic underlying condition reference set",
  "extension" : [ {
    "valueString" : "HSPC Author",
    "url" : "http://hl7.org/fhir/StructureDefinition/valueset-author"
  }, {
    "valueDate" : "2022-12-15",
    "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate"
  }, {
    "valueDate" : "2020-09-03",
    "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate"
  }, {
    "url" : "http://health-samurai.io/extensions/source",
    "valueCode" : "db"
  } ],
  "status" : "active",
  "id" : "2ea018a5-3c58-492d-a20c-bf904768ef96",
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1181.66",
  "identifier" : [ {
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113762.1.4.1181.66"
  } ],
  "version" : "20200903"
}