FHIR IG Statistics: ValueSet/covid19-underlying-metabolic-condition-value-set

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{
  "resourceType": "ValueSet",
  "id": "covid19-underlying-metabolic-condition-value-set",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "url": "http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-metabolic-condition-value-set",
  "version": "1.0.0",
  "name": "COVID19UnderlyingMetabolicConditionVS",
  "title": "COVID-19 metabolic underlying condition reference set",
  "status": "active",
  "date": "2022-07-25T12:22:40+00:00",
  "publisher": "HL7 International - Clinical Information Modeling Initiative",
  "contact": [
    {
      "name": "HL7 International - Clinical Information Modeling Initiative",
      "telecom": [
        {
          "system": "url",
          "value": "http://hl7.org/Special/committees/cimi"
        }
      ]
    },
    {
      "name": "Logica",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.logicahealth.org/"
        }
      ]
    },
    {
      "name": "HL7",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.hl7.org"
        }
      ]
    }
  ],
  "description": "A set of codes that describe underlying metabolic conditions for COVID19",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US",
          "display": "United States of America"
        }
      ]
    }
  ],
  "copyright": "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "267454002",
            "display": "Acatalasemia (disorder)"
          },
          {
            "code": "238069004",
            "display": "Acyl-coenzyme A oxidase deficiency (disorder)"
          },
          {
            "code": "363732003",
            "display": "Addison's disease (disorder)"
          },
          {
            "code": "386584007",
            "display": "Adrenal cortical hypofunction (disorder)"
          },
          {
            "code": "237735008",
            "display": "Adrenal Cushing's syndrome (disorder)"
          },
          {
            "code": "65389002",
            "display": "Adrenoleukodystrophy (disorder)"
          },
          {
            "code": "700463002",
            "display": "Alpha-methylacyl-CoA racemase deficiency disorder (disorder)"
          },
          {
            "code": "54954004",
            "display": "Aspartylglucosaminuria (disorder)"
          },
          {
            "code": "238068007",
            "display": "Bifunctional peroxisomal enzyme deficiency (disorder)"
          },
          {
            "code": "128289001",
            "display": "Chronic metabolic disorder (disorder)"
          },
          {
            "code": "7573000",
            "display": "Classical phenylketonuria (disorder)"
          },
          {
            "code": "35691006",
            "display": "Combined deficiency of sialidase AND beta galactosidase (disorder)"
          },
          {
            "code": "237751000",
            "display": "Congenital adrenal hyperplasia (disorder)"
          },
          {
            "code": "419097006",
            "display": "Danon disease (disorder)"
          },
          {
            "code": "124302001",
            "display": "Deficiency of galactokinase (disorder)"
          },
          {
            "code": "124437004",
            "display": "Deficiency of glucose-6-phosphatase (disorder)"
          },
          {
            "code": "124335006",
            "display": "Deficiency of phosphoglycerate kinase (disorder)"
          },
          {
            "code": "124675005",
            "display": "Deficiency of phosphoglycerate mutase (disorder)"
          },
          {
            "code": "387817006",
            "display": "Deficiency of phosphorylase b kinase (disorder)"
          },
          {
            "code": "124329006",
            "display": "Deficiency of phosphorylase kinase (disorder)"
          },
          {
            "code": "46635009",
            "display": "Diabetes mellitus type 1 (disorder)"
          },
          {
            "code": "44054006",
            "display": "Diabetes mellitus type 2 (disorder)"
          },
          {
            "code": "73211009",
            "display": "Diabetes mellitus (disorder)"
          },
          {
            "code": "45744005",
            "display": "Disorder of mineral metabolism (disorder)"
          },
          {
            "code": "238059005",
            "display": "Disorder of peroxisomal function (disorder)"
          },
          {
            "code": "238006008",
            "display": "Disorder of purine and pyrimidine metabolism (disorder)"
          },
          {
            "code": "30171000",
            "display": "Disorder of adrenal gland (disorder)"
          },
          {
            "code": "73132005",
            "display": "Disorder of parathyroid gland (disorder)"
          },
          {
            "code": "399244003",
            "display": "Disorder of pituitary gland (disorder)"
          },
          {
            "code": "190680002",
            "display": "Disorders of amino acid transport and metabolism (disorder)"
          },
          {
            "code": "16652001",
            "display": "Fabry's disease (disorder)"
          },
          {
            "code": "79935000",
            "display": "Farber's lipogranulomatosis (disorder)"
          },
          {
            "code": "717276003",
            "display": "Folinic acid responsive seizure syndrome (disorder)"
          },
          {
            "code": "20052008",
            "display": "Fructose-1,6-bisphosphate aldolase B deficiency (disorder)"
          },
          {
            "code": "28183005",
            "display": "Fructose-biphosphatase deficiency (disorder)"
          },
          {
            "code": "190745006",
            "display": "Galactosemia (disorder)"
          },
          {
            "code": "192782005",
            "display": "Galactosylceramide beta-galactosidase deficiency (disorder)"
          },
          {
            "code": "190794006",
            "display": "Glucosylceramide beta-glucosidase deficiency (disorder)"
          },
          {
            "code": "235908005",
            "display": "Glycogen storage disease type IX (disorder)"
          },
          {
            "code": "41527003",
            "display": "Glycogen storage disease type VIII (disorder)"
          },
          {
            "code": "37666005",
            "display": "Glycogen storage disease type X (disorder)"
          },
          {
            "code": "717821004",
            "display": "Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)"
          },
          {
            "code": "7265005",
            "display": "Glycogen storage disease, type I (disorder)"
          },
          {
            "code": "274864009",
            "display": "Glycogen storage disease, type II (disorder)"
          },
          {
            "code": "66937008",
            "display": "Glycogen storage disease, type III (disorder)"
          },
          {
            "code": "11179002",
            "display": "Glycogen storage disease, type IV (disorder)"
          },
          {
            "code": "55912009",
            "display": "Glycogen storage disease, type V (disorder)"
          },
          {
            "code": "29291001",
            "display": "Glycogen storage disease, type VI (disorder)"
          },
          {
            "code": "89597008",
            "display": "Glycogen storage disease, type VII (disorder)"
          },
          {
            "code": "237964009",
            "display": "Glycogen synthase deficiency (disorder)"
          },
          {
            "code": "61598006",
            "display": "Glycogenosis with glucoaminophosphaturia (disorder)"
          },
          {
            "code": "238025006",
            "display": "GM1 gangliosidosis (disorder)"
          },
          {
            "code": "353295004",
            "display": "Graves' disease (disorder)"
          },
          {
            "code": "21983002",
            "display": "Hashimoto thyroiditis (disorder)"
          },
          {
            "code": "111578003",
            "display": "Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)"
          },
          {
            "code": "66999008",
            "display": "Hyperparathyroidism (disorder)"
          },
          {
            "code": "10649000",
            "display": "Hyperpituitarism (disorder)"
          },
          {
            "code": "34486009",
            "display": "Hyperthyroidism (disorder)"
          },
          {
            "code": "36976004",
            "display": "Hypoparathyroidism (disorder)"
          },
          {
            "code": "74728003",
            "display": "Hypopituitarism (disorder)"
          },
          {
            "code": "40930008",
            "display": "Hypothyroidism (disorder)"
          },
          {
            "code": "70199000",
            "display": "I-cell disease (disorder)"
          },
          {
            "code": "86095007",
            "display": "Inborn error of metabolism (disorder)"
          },
          {
            "code": "238062008",
            "display": "Infantile Refsum's disease (disorder)"
          },
          {
            "code": "18756002",
            "display": "Juvenile GM1 gangliosidosis (disorder)"
          },
          {
            "code": "65524005",
            "display": "Mannosidosis (disorder)"
          },
          {
            "code": "27718001",
            "display": "Maple syrup urine disease (disorder)"
          },
          {
            "code": "69463008",
            "display": "Maroteaux-Lamy syndrome (disorder)"
          },
          {
            "code": "237602007",
            "display": "Metabolic syndrome X (disorder)"
          },
          {
            "code": "396338004",
            "display": "Metachromatic leucodystrophy (disorder)"
          },
          {
            "code": "725296006",
            "display": "Mucolipidosis type IV (disorder)"
          },
          {
            "code": "75610003",
            "display": "Mucopolysaccharidosis type I (disorder)"
          },
          {
            "code": "65327002",
            "display": "Mucopolysaccharidosis type I-H (disorder)"
          },
          {
            "code": "26745009",
            "display": "Mucopolysaccharidosis type I-H/S (disorder)"
          },
          {
            "code": "70737009",
            "display": "Mucopolysaccharidosis type II (disorder)"
          },
          {
            "code": "73123008",
            "display": "Mucopolysaccharidosis type I-S (disorder)"
          },
          {
            "code": "43916004",
            "display": "Mucopolysaccharidosis type VII (disorder)"
          },
          {
            "code": "378007",
            "display": "Morquio syndrome (disorder)"
          },
          {
            "code": "238061001",
            "display": "Neonatal adrenoleucodystrophy (disorder)"
          },
          {
            "code": "783717008",
            "display": "Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder)"
          },
          {
            "code": "5335002",
            "display": "Phosphoenolpyruvate carboxykinase deficiency (disorder)"
          },
          {
            "code": "25362006",
            "display": "Phytanic acid storage disease (disorder)"
          },
          {
            "code": "65520001",
            "display": "Primary hyperoxaluria, type I (disorder)"
          },
          {
            "code": "65764006",
            "display": "Pseudo-Hurler polydystrophy (disorder)"
          },
          {
            "code": "734434007",
            "display": "Pyridoxine-dependent epilepsy (disorder)"
          },
          {
            "code": "46683007",
            "display": "Pyruvate dehydrogenase complex deficiency (disorder)"
          },
          {
            "code": "23849003",
            "display": "Sandhoff disease (disorder)"
          },
          {
            "code": "88393000",
            "display": "Sanfilippo syndrome (disorder)"
          },
          {
            "code": "38795005",
            "display": "Sialidosis (disorder)"
          },
          {
            "code": "58459009",
            "display": "Sphingomyelin/cholesterol lipidosis (disorder)"
          },
          {
            "code": "34420000",
            "display": "Storage disease (disorder)"
          },
          {
            "code": "367368009",
            "display": "Sulfite oxidase deficiency (disorder)"
          },
          {
            "code": "111385000",
            "display": "Tay-Sachs disease (disorder)"
          },
          {
            "code": "264580006",
            "display": "Thyroid dysfunction (disorder)"
          },
          {
            "code": "8849004",
            "display": "Uridine diphosphate glucose-4-epimerase deficiency (disorder)"
          },
          {
            "code": "88469006",
            "display": "Zellweger syndrome (disorder)"
          }
        ]
      }
    ]
  }
}