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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.23.0 (125 ms)

Package us.nlm.vsac
Type ValueSet
Id Id
FHIR Version R4
Source http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.526.3.1463/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1463
Version 20210219
Status active
Date 2021-02-19T01:00:28-05:00
Name HereditaryRetinalDystrophies
Title Hereditary Retinal Dystrophies
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to represent concepts for diagnoses of hereditary retinal dystrophies.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of hereditary retinal or vitreoretinal dystrophies, including Usher syndrome.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.')

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://snomed.info/sct SNOMED codes used in this IG
http://snomed.info/sct veri
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1671 Hereditary Retinal Dystrophies
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1673 Hereditary Retinal Dystrophies


Source

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  "text" : {
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}

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