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FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1146.2153

Packageus.nlm.vsac
TypeValueSet
Id2.16.840.1.113762.1.4.1146.2153
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2153/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2153
Version20240123
Statusactive
Date2024-01-23T01:10:32-05:00
NamePrimaryCongenitalHypothyroidismDisordersSNOMED
TitlePrimary Congenital Hypothyroidism (Disorders) (SNOMED)
Realmus
Authorityhl7
Purpose(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Primary Congenital Hypothyroidism regardless of the clinical presentation of the condition.),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Primary Congenital Hypothyroidism.),(Exclusion Criteria: None)

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)
sctSNOMED codes used in this IG
sctveri

Narrative

No narrative content found in resource

Source

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