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Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1146.2578",
  "meta": {
    "versionId": "8",
    "lastUpdated": "2025-06-21T01:03:03.000-04:00",
    "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"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
      "valueContactDetail": {
        "name": "CSTE Author"
      }
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-keyWord",
      "valueString": "Homocystinuria,Trigger"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2025-06-21"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2025-06-21"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2578",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1146.2578"
    }
  ],
  "version": "20250621",
  "name": "HomocystinuriaDisordersSNOMED",
  "title": "Homocystinuria (Disorders) (SNOMED)",
  "status": "active",
  "date": "2025-06-21T01:03:03-04:00",
  "publisher": "CSTE Steward",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US"
        }
      ]
    }
  ],
  "purpose": "(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Homocystinuria regardless of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Homocystinuria),(Exclusion Criteria: None)",
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            "code": "11282001",
            "display": "Homocystinuria (disorder)"
          },
          {
            "code": "1260398005",
            "display": "Dystonia due to homocystinuria (disorder)"
          },
          {
            "code": "1296847007",
            "display": "Methylcobalamin deficiency type cblE (disorder)"
          },
          {
            "code": "28093001",
            "display": "Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria (disorder)"
          },
          {
            "code": "360373000",
            "display": "Homocystinuria vitamin B12-responsive type III (disorder)"
          },
          {
            "code": "721187005",
            "display": "Methylcobalamin deficiency type cbl G (disorder)"
          },
          {
            "code": "721225009",
            "display": "Homocystinuria without methylmalonic aciduria (disorder)"
          },
          {
            "code": "80887004",
            "display": "Inherited methylmalonic acidemia AND homocystinuria (disorder)"
          }
        ]
      }
    ]
  },
  "expansion": {
    "identifier": "urn:uuid:fd8db5f1-f572-4c58-950f-e18f490e555c",
    "timestamp": "2025-11-24T13:29:39-05:00",
    "total": 8,
    "contains": [
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        "version": "http://snomed.info/sct/731000124108/version/20250901",
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    ]
  }
}