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FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1146.2500

Packageus.nlm.vsac
TypeValueSet
Id2.16.840.1.113762.1.4.1146.2500
FHIR VersionR4
Sourcehttp://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2500/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2500
Version20250218
Statusactive
Date2025-02-18T01:09:31-05:00
NameRenalAgenesisOrHypoplasiaDisordersSNOMED
TitleRenal Agenesis or Hypoplasia (Disorders) (SNOMED)
Realmus
Authorityhl7
Purpose(Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Renal Agenesis or Hypoplasia regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Renal agenesis, dysgenesis, aplasia, hypoplasia, Potter syndrome secondary to renal agenesis/hypoplasia),(Exclusion Criteria: Cystic renal dysplasia, cystic kidney disease, multicystic kidney, multicystic dysplastic kidney, polycystic kidney, renal cysts, renal dysplasia, small kidney)

Resources that use this resource

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Resources that this resource uses

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

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Source

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