ValueSet-2.16.840.1.113883.3.526.2.1673

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113883.3.526.2.1673
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1673
version20210219
statusactive
publisherAmerican Academy of Ophthalmology Steward
nameHereditaryRetinalDystrophies
titleHereditary Retinal Dystrophies
date2021-02-19T01:00:28-05:00
experimentalfalse
Usages

This value set contains 19 concepts

Code System Display
   15059000 http://snomed.info/sct Retinal dystrophy in systemic lipidosis (disorder)
   192788009 http://snomed.info/sct Retinal dystrophy in cerebroretinal lipidosis (disorder)
   193400007 http://snomed.info/sct Hereditary retinal dystrophies in lipidoses (disorder)
   193409008 http://snomed.info/sct Hyaline retinal dystrophy (disorder)
   193415008 http://snomed.info/sct Tapetoretinal dystrophy (disorder)
   232052009 http://snomed.info/sct Autosomal dominant retinitis pigmentosa (disorder)
   232053004 http://snomed.info/sct Autosomal recessive retinitis pigmentosa (disorder)
   232056007 http://snomed.info/sct Progressive rod dystrophy (disorder)
   232057003 http://snomed.info/sct Usher syndrome type 1 (disorder)
   232058008 http://snomed.info/sct Usher syndrome type 2 (disorder)
   267613004 http://snomed.info/sct Progressive cone dystrophy (without rod involvement) (disorder)
   28835009 http://snomed.info/sct Retinitis pigmentosa (disorder)
   312917007 http://snomed.info/sct Cone dystrophy (disorder)
   313003009 http://snomed.info/sct Rod dystrophy (disorder)
   41799005 http://snomed.info/sct Hereditary retinal dystrophy (disorder)
   57838006 http://snomed.info/sct Retinitis pigmentosa-deafness syndrome (disorder)
   764939004 http://snomed.info/sct Fundus albipunctatus (disorder)
   79556007 http://snomed.info/sct Vitreoretinal dystrophy (disorder)
   80328002 http://snomed.info/sct Progressive cone-rod dystrophy (disorder)

Produced 08 Sep 2023