COVID19 SNOMED Value Set for Muscular Dystrophy

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  "date" : "2023-06-21T18:16:37-04:00",
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  "purpose" : "(Clinical Focus: This set of values contains terms related to muscular dystrophy and is listed as a neurologic disorder on the CDC SARS-CoV-2 hospitalization surveillance case report form.),(Data Element Scope: ),(Inclusion Criteria: Includes autosomal dominant and recessive limb girdle muscular dystrophy, Becker muscular dystrophy, congenital muscular dystophies, Duchenne muscular dystrophy, X-linked muscular dystrophy and other hereditary and idiopathic dystrophies.),(Exclusion Criteria: )",
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      "code" : "1010712009",
      "display" : "Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder)",
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      "system" : "http://snomed.info/sct",
      "code" : "111501005",
      "display" : "Congenital hereditary muscular dystrophy (disorder)",
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      "system" : "http://snomed.info/sct",
      "code" : "111502003",
      "display" : "Fukuyama congenital muscular dystrophy (disorder)",
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      "code" : "111503008",
      "display" : "Merosin deficient congenital muscular dystrophy (disorder)",
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    }, {
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      "code" : "111504002",
      "display" : "Walker-Warburg congenital muscular dystrophy (disorder)",
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      "code" : "111505001",
      "display" : "Muscle-eye-brain disease, congenital muscular dystrophy (disorder)",
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      "code" : "111506000",
      "display" : "Distal muscular dystrophy, Miyoshi type (disorder)",
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      "code" : "1172703004",
      "display" : "Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 (disorder)",
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      "display" : "Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder)",
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