| 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
FHIR