Package | us.nlm.vsac |
Type | ValueSet |
Id | 2.16.840.1.113762.1.4.1146.2500 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2500/expansion |
URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2500 |
Version | 20250218 |
Status | active |
Date | 2025-02-18T01:09:31-05:00 |
Name | RenalAgenesisOrHypoplasiaDisordersSNOMED |
Title | Renal Agenesis or Hypoplasia (Disorders) (SNOMED) |
Realm | us |
Authority | hl7 |
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) |
No resources found
CodeSystem | |
sct | SNOMED CT (all versions) |
sct | SNOMED codes used in this IG |
sct | veri |
No narrative content found in resource