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FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1219.15

Packageus.nlm.vsac
TypeValueSet
Id2.16.840.1.113762.1.4.1219.15
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1219.15/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.15
Version20220315
Statusactive
Date2022-03-15T01:04:14-04:00
NameCysticFibrosisLungDisease
TitleCystic Fibrosis Lung Disease
Realmus
Authorityhl7
Purpose(Clinical Focus: Cystic fibrosis lung disease),(Data Element Scope: Cystic fibrosis lung disease which may require medical equipment such as oxygen therapy, as defined by U.S. Centers for Medicare and Medicaid.),(Inclusion Criteria: Cystic fibrosis, inherited or acquired),(Exclusion Criteria: Imotile ciliary syndrome)

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Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)
icd-10-cmInternational Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
sctSNOMED codes used in this IG
sctveri
icd-10-cmInternational Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
ValueSet
2.16.840.1.113762.1.4.1219.13Cystic Fibrosis Lung Disease ICD10CM
2.16.840.1.113762.1.4.1219.14Cystic Fibrosis Lung Disease SNOMEDCT

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