| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113883.3.526.3.1463 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1463 |
| version | 20210219 |
| status | active |
| publisher | American Academy of Ophthalmology Steward |
| name | HereditaryRetinalDystrophies |
| title | Hereditary Retinal Dystrophies |
| date | 2021-02-19T01:00:28-05:00 |
| experimental | false |
| Usages | (none) |
This value set contains 25 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) |
| H35.50 | http://hl7.org/fhir/sid/icd-10-cm | Unspecified hereditary retinal dystrophy |
| H35.51 | http://hl7.org/fhir/sid/icd-10-cm | Vitreoretinal dystrophy |
| H35.52 | http://hl7.org/fhir/sid/icd-10-cm | Pigmentary retinal dystrophy |
| H35.53 | http://hl7.org/fhir/sid/icd-10-cm | Other dystrophies primarily involving the sensory retina |
| H35.54 | http://hl7.org/fhir/sid/icd-10-cm | Dystrophies primarily involving the retinal pigment epithelium |
| H36 | http://hl7.org/fhir/sid/icd-10-cm | Retinal disorders in diseases classified elsewhere |
Produced 08 Sep 2023